Cresun Medical Components
Sheet metal, CNC machining, surface treatment and equipment assembly in supplier material. Registry checked; factory audit, certified scope and device approvals remain open.
Parts and assembly services, not an assumed device approval.
Sheet-metal structures & enclosures
The supplier brochure describes sheet-metal manufacturing and shows workshop equipment. Request thickness range, material grades, drawing revision and dimensional acceptance limits for your part.
Precision-machined components
Brochure imagery shows machining workshops and inspection instruments. Tolerances, calibrated machine capability and sample inspection reports remain to be supplied.
Surface treatment
The brochure includes a surface-treatment line. Confirm pretreatment, coating specification, adhesion/corrosion tests, subcontracting and material traceability for the specific order.
Equipment assembly services
Assembly workshop images and imaging-equipment examples appear in the brochure. These establish a supplier claim, not ownership of device designs, customer authorization or market clearance.
Supplier brochure workshop evidence.
Supplier-provided images from the reviewed brochure. No independent site audit or ownership verification is implied.
What the registry confirms, and what stays open.
Manufacturing in registered scope
The registry includes general equipment, electromechanical equipment and hardware manufacturing. It also includes goods import/export and import/export agency.
Documented workshop imagery
Five brochure pages show assembly, machining, sheet-metal fabrication, surface treatment and quality-testing scenes. Photos are supplier-provided; equipment ownership and present operating status need audit confirmation.
Company versus group
Group affiliation and shared resources are brochure statements. Confirm which legal entity owns the production equipment and signs each contract.
Capacity figures require scope
The brochure states 15,000 m² and more than 70 employees; the registry records 16 social-insurance participants. These measure different things and need a dated entity-specific explanation.
Traceability is the qualification gate
Ask for material certificates, first-article dimensional results, process flow, change control and calibration records before approving production.
No medical clearance inferred
General manufacturing and first-class medical-device sales wording do not establish authorization for a specific finished imaging device or accessory.
Related-entity risk signals
The registry risk feed records no self-risk items and four surrounding-risk items linked to a corporate shareholder: service-of-process notices, an administrative-penalty signal and an environmental-penalty signal. These are not findings against this entity; underlying cases and relevance need independent checking.
What was checked — and what the check found.
CMH Verified on this page means the business registry was checked, not a factory audit, ISO certification, product approval or endorsement of medical performance. Supplier imagery and self-reported figures stay subject to document and site verification.
A manufacturing entity, with brochure claims kept separate.
The legal entity 惠州市卡瑞森医疗科技有限公司 is active in the registry, with a registration date of 11 May 2023 and a former registered name 惠州市常准医疗科技有限公司. The supplied brochure uses the English name Huizhou Cresun Medical Technology Co., Ltd.
The brochure presents a chain from sheet metal and precision machining through surface treatment and assembly. It also shows inspection equipment. No independent dimensional report, certificate or production audit was part of this review.
The brochure describes a 2022 start while the legal entity was registered in 2023. Ask whether 2022 refers to a predecessor team or group operation; neither date is silently substituted for the other.
A registry history, and the evidence still needed.
Legal registration
Current registry records 11 May 2023; the brochure’s 2022 history needs entity clarification.
Supplier material reviewed
21-page brochure with production and inspection imagery supplied to CMH.
Project qualification
Clarify legal roles, certificates, sample quality, capacity and destination-market responsibilities.
Where this capability fits, subject to project qualification.
Medical-equipment OEM procurement
Buyers seeking fabricated housings, frames or machined parts to controlled drawings, with an agreed quality plan.
Engineering and supply-chain teams
Pilot-to-series sourcing where sample sign-off and revision control precede volume commitments.
Assembly outsourcing
Only after product owner, manufacturing scope, final testing and release responsibilities are allocated in writing.
Veterinary imaging projects
Brochure examples include animal imaging; scope and destination requirements must be assessed separately from human-use devices.
Sourcing guides for this category
What Documents to Request From a Chinese Supplier Before Your First Order
How to Write a Product Spec Sheet for a Chinese Factory
Product Inspection in China Before Shipment: A Buyer's Guide
The 27-Point China Factory Audit Checklist
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Frequently Asked Questions
Does CMH Verified mean the products are FDA approved?
No. It means the business registry was checked. FDA registration/listing is not approval, and no product clearance was verified.
Are components automatically finished medical devices?
No blanket rule applies. Intended use, functionality and accessory status matter. FDA notes some diagnostic X-ray components are finished devices; confirm each scope with the responsible manufacturer.
What should an RFQ include?
Drawing revision, materials, finish, critical dimensions, quantity, intended use, traceability and first-article acceptance requirements.
Has ISO 13485 been verified?
No certificate original, issuer verification and certified legal-entity/site scope were supplied in this review.
Can the brochure customer names be used as references?
Not without authorization and evidence. Ask for a redacted project case and customer-approved reference.
Why do employee and start-date figures differ?
The brochure states a 2022 start and more than 70 employees; the registry shows a 2023 registration and 16 social-insurance participants. Ask for the legal-entity versus group and date/statistical scope.
What delivery terms apply?
MOQ, samples, lead times, incoterms and payment have not been supplied. Obtain an order-specific agreement.
How should European projects be qualified?
Allocate the legal manufacturer and importer responsibilities. EU guidance allows supplier/subcontractor audits where appropriate; an ISO certificate alone is not enough.
Talk to Cresun Medical Components directly.
Send a drawing revision, material and surface finish, critical tolerances, annual volume, pilot quantity and intended use. Confirm whether you require a component, functional accessory or finished device before agreeing compliance and acceptance responsibilities.