Sanming Plastics
Plastic products, Class I–III medical devices and non-medical masks from a Jiexi company designated as a National High-tech Enterprise — production scope, licences and government designations stated up front.
Plastics, devices, masks and textiles.
Plastic Products (塑料制品)
The company’s primary registered activity is the manufacture and sale of plastic products. No product catalogue or specification has been supplied. Ask which plastic forms are produced (sheet, profile, moulded part, container, packaging), what polymers are used, and for material data sheets.
Medical Devices — Class I (第一类医疗器械)
Class I medical device production and sales are in the general-item scope (no special licence required for Class I in China). The specific device categories have not been disclosed. Ask which Class I devices are manufactured, for the product registration and listing numbers, and for any test reports.
Medical Devices — Class II/III (第二/三类医疗器械)
The company holds licences for Class II and Class III medical-device production and distribution. These are regulated products requiring NMPA (National Medical Products Administration) approval in China and equivalent regulatory clearance in export markets. Ask which specific devices are made, for the NMPA registration certificates and production licence numbers.
Non-Medical Masks (日用口罩)
Production and sale of daily-use non-medical masks are in scope. These are consumer products, not medical-grade. For export, they may need to meet standards such as GB/T 32610 (China), EN 149 (EU) or NIOSH 42 CFR 84 (US) depending on the claimed protection level and destination. Ask for test reports and the applicable standard.
Industrial Textiles & Synthetic Fibres
The scope includes industrial textile products manufacturing and sales, synthetic fibre manufacturing, and synthetic materials sales. No further detail has been provided. Ask which textile products are made, what fibres are produced, and for what end uses.
What Has Not Been Supplied
There is no company website, no product catalogue, no material data sheet, no test report and no certificate on record. No product photos were provided. This page describes product families from the registered scope; details will be added when documents arrive.
What the registry confirms, and what stays open.
Plastics Manufacturing in Scope
The registered scope includes 塑料制品制造 (plastic products manufacturing) and 塑料制品销售 (plastic products sales) under general items. The registered industry classification is rubber and plastic products (橡胶和塑料制品业), sub-category plastics (塑料制品业). The company also has special equipment manufacturing (non-licensed) in scope.
Licensed Medical-Device Production
Under licensed items, the company holds permits for Class II medical-device production (第二类医疗器械生产), Class III medical-device production (第三类医疗器械生产) and Class III medical-device distribution (第三类医疗器械经营). These are the highest-tier manufacturing licences in China’s medical-device regulatory framework. The specific device categories covered by these licences have not been disclosed.
High-tech Enterprise & Specialised-Innovative SME
The company is tagged as a National High-tech Enterprise (高新技术企业) and a Specialised-Innovative SME (专精特新中小企业). The High-tech Enterprise designation requires passing a government review of R&D spending, IP ownership and revenue from high-tech products. The Specialised-Innovative SME designation recognises focused expertise in a niche market. Both are recorded in the registry read.
Capital Fully Paid In
Registered capital is RMB 6,000,000 and paid-in capital is also RMB 6,000,000 — the two match in full. The company is a limited liability company (natural person investment or holding), registered on 2009-05-13; the record was last approved on 12 November 2024.
11 Insured Staff on Record
The registry read records 11 people on social insurance at this entity. The company is classified as a micro-enterprise (小微企业) and also as above-scale industrial (规模以上工业). No employee count was stated by the company.
No Import/Export in Registered Scope
The registered scope does not include import or export of goods. If the company exports, it would need to apply for an export filing (对外贸易经营者备案) separately, or export through a trading company. This is common for manufacturing-focused entities in China. Ask the company about its export arrangements.
Historical Court Records — All as Plaintiff
The risk scan read on 2026-10-04 lists: self risk 0, nearby risk 0. Historical records: 2 case filings and 1 hearing notice (all as plaintiff, i.e. the company was the one suing), and 1 judgment document in a sales-contract dispute. Advisory items: 2 tax-rating changes. No abnormal-operation listing or serious-violation listing was found.
What was checked — and what the check found.
The registry read is done: status, scope, capital, insured headcount and court records come from an official registry source read on 2026-10-04 and are quoted as recorded. The company is designated as a National High-tech Enterprise and a Specialised-Innovative SME. Its licensed scope covers Class II and III medical-device production and distribution — the highest-tier manufacturing licences in China’s medical-device framework. No specific device categories, registration numbers, product catalogues, test reports or certificates have been supplied. This page is updated when documents arrive.
Plastic products and medical devices since 2009, read off registry.
Sanming Plastics is Jiexi County Sanming Plastic Co., Ltd. (揭西县三明塑料有限公司), registered on 13 May 2009 in Jiexi County, Guangdong, with registered and paid-in capital of RMB 6,000,000. An official registry read on 2026-10-04 confirms active (存续) status and a scope covering plastic products manufacturing, Class I medical-device production (general) and Class II/III medical-device production and distribution (licensed), as well as non-medical masks, industrial textiles and synthetic fibres.
The company is designated as a National High-tech Enterprise (高新技术企业) and a Specialised-Innovative SME (专精特新中小企业). These government designations reflect R&D capability and niche expertise respectively. The registry records 11 insured staff; the company is classified as a micro-enterprise and as above-scale industrial. Its diversified scope also covers EV charging infrastructure and property management.
No product specifications, material data sheets, test reports, certificates or photos have been supplied. The product families described on this page come entirely from the registered scope; details will be added when documents arrive.
Registered in 2009, government-designated high-tech.
Company registered
Registered on 13 May 2009 in Jiexi County, with a scope initially covering plastic products manufacturing and sales (registry read).
Over 15 years in operation
The scope expanded to include medical devices (Class I–III), non-medical masks, industrial textiles, synthetic fibres and EV charging infrastructure. The company obtained High-tech Enterprise and Specialised-Innovative SME designations. Capital fully paid in at RMB 6 million. Record last approved 12 November 2024.
Registry read · joins CMH
Listed from an official registry read on 2026-10-04; product catalogues, specifications, certificates and medical-device registration numbers remain open.
Where these products typically go.
Medical & Healthcare
Medical devices (Class I through III) and non-medical masks for healthcare facilities, pharmacies and consumer health.
Consumer Products
Daily-use masks and plastic consumer goods for domestic and export markets.
Industrial & Packaging
Plastic products for industrial use, packaging, and the downstream of synthetic fibres and materials.
Textiles & Technical Fabrics
Industrial textile products and synthetic-fibre-based materials for filtration, protection or reinforcement.
Automotive & Infrastructure
The scope includes EV charging-station operation and charging-pile sales, alongside equipment manufacturing, suggesting industrial diversification.
Sourcing guides for this category
The 27-Point China Factory Audit Checklist
Product Inspection in China Before Shipment: A Buyer's Guide
How to Request a Sample from a Chinese Factory (Without Getting Burned)
What Documents to Request From a Chinese Supplier Before Your First Order
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Frequently Asked Questions
What does Sanming Plastics make?
By its registered scope: plastic products, Class I through III medical devices, non-medical daily-use masks, industrial textile products and synthetic fibres. No product catalogue, specification sheet or photos have been supplied, so specific product lines are not confirmed.
Is this listing CMH-verified?
Yes, on the registry check: an official registry read on 2026-10-04 confirms active status, a scope that includes plastic products manufacturing and licensed medical-device production, fully paid-in capital of RMB 6 million, and designations as a High-tech Enterprise and Specialised-Innovative SME. It does not confirm any product specification, grade or test result.
Does the company export?
The registered scope does not include import or export of goods. This does not mean the company cannot export; it may have an export filing or work through a trading company. Ask the company directly.
What are the government designations?
The registry tags this company as a National High-tech Enterprise and a Specialised-Innovative SME. The High-tech Enterprise designation is reviewed every three years and requires the company to demonstrate R&D spending, intellectual-property ownership and revenue from high-tech products. The Specialised-Innovative SME designation recognises companies with focused expertise in a niche. Both are positive signals but are not product-level certifications.
Are there court records?
Historical records show 2 case filings, 1 court hearing notice and 1 judgment document in a sales-contract dispute. In all cases the company was the plaintiff (the one bringing suit). There are no own-risk items and no abnormal-operation listings. Advisory items include 2 tax-rating changes.
What regulations apply to plastic products for export?
For the United States: consumer plastic products fall under CPSIA; children’s products require third-party testing. California Proposition 65 lists lead and certain phthalates. For the EU: REACH Annex XVII restricts phthalates, lead and cadmium in plastics. Food-contact plastics are regulated under FDA 21 CFR (US) or Regulation (EU) 10/2011. Ask for test reports specific to the product and its end use.
What about medical-device export regulations?
Medical devices for the US require FDA 510(k) clearance or PMA depending on classification. For the EU, devices need CE marking under the Medical Device Regulation (EU) 2017/745 (MDR). Both require conformity assessment, quality-management-system certification (typically ISO 13485) and device registration in the destination market. The Chinese NMPA licence alone does not grant access to foreign markets. Ask for the specific device registration numbers and any ISO 13485 certificate.
Which HS codes usually apply?
Plastic products generally fall under HS Chapter 39 (e.g. 3926 for other articles of plastics, 3923 for packaging articles, 3920/3921 for plates and sheets). Medical devices typically fall under HS Chapter 90 (e.g. 9018 for medical instruments). Non-medical masks may fall under 6307.90 (other made-up textile articles). Classification depends on the specific product and is decided by customs at import.
Talk to Sanming Plastics directly.
Tell us the product type (plastic product, medical device, mask or textile), material, specifications, intended use, destination market and the quantity. For medical devices, state the classification and intended clinical purpose. Ask for product registration certificates, test reports, material data sheets and the factory address for a site visit.