Hermann Meditech
Fabricante de instrumentos quirúrgicos con certificación ISO 13485 dirigido a adquisiciones médicas europeas.
Hermann Meditech produce instrumentos quirúrgicos con certificación ISO 13485 con énfasis en los requisitos del mercado europeo, incluido el cumplimiento de MDR. La empresa fabrica tijeras quirúrgicas, pinzas, retractores y juegos de instrumentos personalizados para distribuidores médicos y de adquisiciones hospitalarias europeas.
- Type
- brand seeking distribution
- Location
- Sialkot, Pakistan
- Website
- hmeditech.com
- Categories
- Suministros médicos y sanitarios
- Markets
- Alemania, Estados Unidos, Reino Unido, Suiza
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)