- ISO 13485 certified
- 9 categories · 240+ models
- Our own plant in Taiwan
Partners
Become a distribution partner
Medical Master has been in medical devices since 2003 and manufacturing in-house since 2006, supplying over thirty markets through distribution partners. Catalogues and certificates are open to download; spec sheets, regulatory notices and the dealer price list are for approved partners.
Why work with us
Our own plant, our own lead times
Fabrication, welding, coating and assembly are all in house — nothing is subcontracted.
Import registration support
Declarations of conformity, material certificates and test reports for your local registration.
OEM / ODM customisation
Dimensions, rails, castors and export packaging adapted to your market and regulations.
Apply for a dealer account
Once approved you can download spec sheets, installation manuals and the dealer price list. We usually reply within one or two working days.
Already a partner?
Document access
Public
No sign-in
Product catalogues and ISO 13485 / FDA certificates.
B-level
Approved partner
Regulatory registration notices, spec sheets and installation manuals.
A-level
Appointed distributor
Dealer price list, MOQ and new product previews.
Catalogue downloads
You can also browse the nine product categories or see how to independently verify our certifications.
MEB-900 Electric Bed Series Catalogue Public
Full specifications, function diagrams and option list for the MEB-903/904 range.
MET-6000/3000 Patient Stretcher Catalogue Public
Transport, trauma, pediatric and transfer stretchers with full dimensional data.
ISO 13485 Quality Management Certificate Public
Issued by DNV, covering Medical-Master and Summit Care.
US FDA Establishment Registration Public
FDA Registration No. 3006554924. Registration is not approval; the FDA does not endorse products.
EU MDR Registration Notice: Medical Bed B-level
EU MDR registration notification (RPS_2847_2025).
EU MDR Registration Notice: Treatment Table B-level
EU MDR registration notification (RPS_2848_2025).
EU MDR Registration Notice: Patient Stretcher B-level
EU MDR registration notification (RPS_2849_2025).
New Product Preview (Confidential) A-level
Next-quarter models and launch schedule. Not for public distribution.
Dealer-only documents are stored outside the web root and streamed only after a permission check — a direct link will not work without signing in.
