Hermann Meditech
ISO 13485-certified surgical instrument manufacturer targeting European medical procurement.
Hermann Meditech produces ISO 13485-certified surgical instruments with an emphasis on European market requirements including MDR compliance. The company manufactures surgical scissors, clamps, retractors, and custom instrument sets for European hospital procurement and medical distributors.
- Type
- brand seeking distribution
- Location
- Sialkot, Pakistan
- Website
- hmeditech.com
- Categories
- Medical & Healthcare Supplies
- Markets
- Germany, United States, United Kingdom, Switzerland
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- registry-id-verified (green), checked 2026-08-19 FBR Active Taxpayer List (Federal Board of Revenue, Pakistan)
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)