Hermann Meditech
Fabricant d’instruments chirurgicaux certifié ISO 13485 ciblant l’approvisionnement médical européen.
Hermann Meditech produit des instruments chirurgicaux certifiés ISO 13485 en mettant l'accent sur les exigences du marché européen, notamment la conformité MDR. La société fabrique des ciseaux chirurgicaux, des pinces, des écarteurs et des ensembles d'instruments personnalisés pour les fournisseurs d'hôpitaux européens et les distributeurs médicaux.
- Type
- brand seeking distribution
- Location
- Sialkot, Pakistan
- Website
- hmeditech.com
- Categories
- Fournitures médicales et de santé
- Markets
- Allemagne, États-Unis, Royaume-Uni, Suisse
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)