Jingying Medical Devices
Purified-water plants, multi-effect WFI distillation and pure steam generators from Kuiwen, Weifang — registered 1996 with goods import/export on the scope. Pressure-vessel tickets and GMP dossiers are the open checks.
Pharma utility systems, built as packages.
Purified-Water Preparation Systems
Pre-treatment (multi-media / activated carbon / softener / guard filter) plus RO/EDI trains sized from the buyer’s raw-water report. Supplier-stated controls: residual chlorine <0.1 ppm, SDI <3, hardness <1.5 ppm after softening; Siemens S7 PLC + HMI, remote diagnostics and a service app. Send a current water analysis with the inquiry — design is water-specific.
Multi-Effect Distillation (WFI)
Supplier-stated six-effect design with three-stage separation (falling-film, gravity, spiral turbulence): outlet 95±1 °C, conductivity ≤0.5 µS/cm, endotoxin 0.01 EU/mL, TOC <50 ppb, steam ratio 0.21, feed ratio 1.08. Ask for the FAT protocol and the endotoxin/TOC test records on a shipped unit.
Pure Steam Generators
Supplier-stated quality: dryness >98%, non-condensable gases <2%, superheat <2 °C — company claims these beat the Chinese national limits. Dual pre-heaters and a feed condenser for energy recovery. Request the dryness and non-condensable test certificates.
Storage & Distribution Loops
Modular tanks with return-loop heat recovery, PID heat exchange, online TOC and conductivity, flow-controlled returns and 3D pipe design. Supplier publishes peak-demand worksheets for sizing. Ask for a loop velocity calculation and slope/passivation reports.
CIP / SIP & Auto-Batching
Skid-mounted CIP/SIP stations and automated batching (concentrate + dilute tanks, load cells, diaphragm valves, zero-dead-leg fittings, side-wall sampling). Supplier-stated one-touch recipes. Request weld logs and endoscope reports for the wetted path.
Process Piping & Installation
On-site piping design and installation to accompany the skids — supplier states P&ID, isometrics, weld maps, passivation and hydostatic test packs in the handover dossier. Confirm the installation crew’s qualifications and who signs the FAT/SAT.
What the registry confirms, and what stays open.
Pharma Equipment Is the Registered Trade
The registry read on 2026-10-07 shows 制药专用设备制造/销售 (pharmaceutical special-equipment manufacturing and sales) and 水资源专用机械设备制造 on the scope. Making drug-plant utilities is a registered business, not a side line.
Export in Its Own Name
The same scope carries 货物进出口 and 技术进出口. The company can contract, invoice and ship in its own name — a real advantage over peers that must borrow a trading company’s papers.
Pressure-Vessel Credentials (stated)
Company-stated: Class I pressure-vessel manufacture plus Class I/II design and manufacture qualifications. These are the tickets that matter for stills and vessels — request the licence scans and validity dates before the first PO.
Scale on the Registry
Registered capital RMB 20 million, paid-in RMB 5 million (registry). 103 social-insurance participants — a real payroll, not a shell. Company-stated headcount is about 180 including 20+ senior technical staff; treat as stated until seen on site.
Validation Pack Experience
Supplier states a full GMP document chain: DQ/DDS/HDS, IQ, OQ, PQ, FAT/SAT, weld logs, endoscope, passivation, riboflavin and risk assessments. Ask for a redacted sample dossier from a past client before you buy the claim.
Pharma Customer Base (stated)
Company-stated: 2,000+ pharmaceutical plants and 700+ hospitals served; equipment exported to 40+ countries including the US, Russia, Egypt, India and Korea. Named domestic groups appear in the company deck; treat third-party names as stated until confirmed with the counterparties.
What was checked — and what the check found.
The registry read is done. On 2026-10-07 the corporate record was pulled from a Chinese enterprise-data provider: the company is active (存续), registered 25 December 1996 in Kuiwen District, Weifang, formerly the medical-appliance works of a local pharmaceutical group. The credit code passes the national check-digit rule. Registered scope covers pharmaceutical special-equipment manufacturing and sales, water-resource special-equipment manufacturing, special-equipment design and manufacture (permit-required), construction, and goods and technology import/export. Registered capital is RMB 20 million with RMB 5 million paid in; 103 social-insurance participants. One tag stays on the record: the company is a small/micro enterprise and carries a judicial-case tag with no case detail published — ask for the nature of that matter in writing. Pressure-vessel design/manufacture qualifications, three-system certificates, the 1958 founding claim, the 61,700 m² site figure, the 180-person headcount and the 2,000+ plant / 700+ hospital track record all come from the company’s own 2024 deck and are labelled stated. ChinaMakersHub does not restate a supplier’s certificate validity on its behalf — we tell you what to ask for.
A Weifang process-equipment works, on the record.
Jingying Medical Devices is the export name of 山东潍坊精鹰医疗器械有限公司 (Shandong Weifang Eagle Medical Appliances Co., Ltd.), a pharmaceutical-utility equipment maker registered in December 1996 on Wenhua South Road, Kuiwen District, Weifang, Shandong. The corporate record was checked against a Chinese enterprise-data provider on 2026-10-07. The company was formerly the medical-appliance works of a local pharmaceutical group — a lineage that matches its current product line of purified-water plants, multi-effect stills and pure-steam generators.
What the company builds is the utility core of a drug plant: raw-water pre-treatment and RO/EDI purified-water trains, six-effect WFI distillation, pure steam generators, storage and distribution loops, CIP/SIP skids and automated batching, plus on-site process piping. That is a project business, not an e-commerce SKU — expect a technical dialogue around your water analysis, target pharmacopoeia and plant layout before a quotation means anything.
What the registry check found is stated plainly. The read on 2026-10-07 confirms an active company with pharmaceutical-equipment manufacturing and goods import/export on the scope — the Verified stamp in the hero is earned on that basis. Registered capital is RMB 20 million of which RMB 5 million is paid in, and 103 people are on social insurance — a real works. Pressure-vessel tickets, the three-system certificates, the site size, the founding-year claim and the customer counts are company-stated until the originals are in your hands. The 2024 deck also lists domestic pharma groups among reference projects; treat third-party names as stated. Contact routes through ChinaMakersHub; direct details are exchanged after first inquiry.
From a 1958 works to a registered maker, facts first.
Works lineage (stated)
The company deck traces the works to 1958 as a medical-appliance plant. The corporate registry carries a later incorporation date and a former name tied to a local pharmaceutical group — treat 1958 as heritage narrative, 1996 as the legal start.
Registered as a limited company
Incorporated 25 December 1996 as a limited company in Kuiwen District, Weifang. Confirmed on the corporate registry, including the former name of a pharmaceutical-group medical-appliance works.
Scope refresh on record
Registry shows a 2022-06-13 update to the current business scope — pharma special equipment, water-resource equipment, special-equipment design/manufacture and goods/technology import/export. Confirmed on the registry read.
Company deck published
The 2024-03 introduction pack presents eight processing centres (including electrochemical polishing and a FAT hall), pressure-vessel tickets, a GMP document chain and a reference list of pharma and hospital projects across 40+ export markets. All company-stated.
Registry read — manufacturing and export confirmed
On 2026-10-07 ChinaMakersHub read the corporate record: active, pharma-equipment manufacturing and import/export on scope, RMB 20m capital / 5m paid-in, 103 insured. Open and stated: pressure-vessel licence originals, certificate validity dates, capacity audit and sample GMP dossiers.
Where these systems go to work.
Generic Drug & API Plants
Purified-water and WFI systems for small-molecule injectables and API workshops. Send the water-source analysis and the pharmacopoeia edition you must meet; ask for endotoxin/TOC test records from a shipped still.
Biologics & Sterile Fill-Finish
Pure steam generators and distribution loops for SIP of sterile paths. Request dryness / non-condensable certificates and a passivation + endoscope report pack for the wetted path.
Hospital & Central Sterile Supply
Compact purified-water and pure-steam packages for CSSD and dialysis support. Confirm footprint, utility loads and local installation support before contracting.
Export Projects (US / EU / CIS / MENA / South Asia)
Company-stated shipments to 40+ countries. For regulated markets, ask for the ASME/CE status of vessels and the English documentation set — the deck is Chinese-first.
Plant Retrofit & Capacity Debottlenecking
Add effects, expand loops or upgrade controls on an existing utility. Send the current P&ID and last validation report; confirm who owns the re-qualification.
Turnkey Utility Packages
Skids + piping + validation documents as one contract. Request a sample document index, a FAT protocol and the SAT acceptance criteria before awarding.
Sourcing guides for this category
Importing from China: The Compliance Checklist by Market
What Documents to Request From a Chinese Supplier Before Your First Order
CE, FCC and Product Certification for China-Made Goods
The 27-Point China Factory Audit Checklist
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Frequently Asked Questions
What does Jingying Medical Devices make?
Pharmaceutical plant utilities, per the company’s 2024 deck and the registered scope: purified-water preparation systems (pre-treatment + RO/EDI), multi-effect WFI distillation units, pure steam generators, storage and distribution loops, CIP/SIP and automated batching skids, and on-site process piping. The registered scope includes pharmaceutical special-equipment manufacturing and sales. Product performance figures on this page are supplier-stated until test records are sighted.
Is Jingying a factory or a trading company?
A registered limited company with pharmaceutical special-equipment manufacturing on the scope and 103 social-insurance participants — a real works. The company states eight processing centres including CNC, automatic welding, electrochemical polishing and a FAT hall, on a 61,700 m² site (stated). Ask for a video walkthrough and the pressure-vessel workshop licence before sizing a project.
Can it export in its own name?
Yes on the registry: the scope carries 货物进出口 and 技术进出口 (goods and technology import/export). The company can contract, invoice and ship in its own name. Company-stated exports to 40+ countries including the US, Russia, Egypt, India and Korea. Confirm Incoterms, currency and who signs the FAT/SAT in the contract.
What certifications does it hold?
Company-stated: Class I pressure-vessel manufacture plus Class I/II design and manufacture qualifications; ISO three-system certificates; various patents and industry awards. No licence or certificate carrying a legible issuer, holder name and validity date was sighted at review — this page does not claim them. Request the originals in the tender pack.
What are the technical figures on the WFI stills?
Supplier-stated for the multi-effect distillation line: six effects, three-stage separation, outlet 95±1°C, conductivity ≤0.5µS/cm, endotoxin 0.01 EU/mL, TOC <50 ppb, steam ratio 0.21 and feed ratio 1.08. Ask for the FAT protocol and the endotoxin/TOC test records on a shipped unit before accepting these numbers for a URS.
What did the ChinaMakersHub registry check find?
Run on 2026-10-07: an active limited company registered 25 December 1996 in Kuiwen District, Weifang; USCC 913707051654465612 check digit passes; scope covers pharmaceutical special-equipment manufacturing and sales, water-resource equipment, special-equipment design/manufacture and goods/technology import/export. Registered capital RMB 20 million / paid-in RMB 5 million. 103 social-insurance participants. Tags: small/micro enterprise and a judicial-case entry with no published detail — ask for the nature of that matter in writing.
Why does the page separate registry facts from deck claims?
Because a 2024 marketing deck is a sales document. The registry confirms identity, scope, capital and payroll; the deck asserts capacity, certificates, site size, founding year and customer counts. Mixing the two is how buyers get surprised. Everything from the deck is marked stated; everything from the registry is marked registry-confirmed.
What should I ask for before the first PO?
In writing: pressure-vessel design and manufacture licence scans with validity dates; three-system certificate scans; a redacted DQ/IQ/OQ/PQ document index from a past project; FAT protocol and acceptance criteria; weld/passivation/endoscope report samples; lead time and liquidated damages; and the install crew’s qualifications. Ask also for the nature of the judicial-case tag on the registry.
Talk to Jingying Medical Devices directly.
Send your water-source analysis, required water quality (Chinese Pharmacopoeia / USP / EP), capacity in L/h, plant layout and the destination market. Ask in the same message for the pressure-vessel design/manufacture licences, the three-system certificates, and a sample DQ/IQ/OQ/PQ document index from a past project. ChinaMakersHub will route the request.