Dr. Frigz International
Producteur OEM/marque privée d'instruments chirurgicaux stériles conformes au MDR.
Le Dr Frigz produit une gamme complète d'instruments chirurgicaux, dentaires et vétérinaires stériles sous accords OEM et sous marque privée. Avec l'enregistrement ISO 13485, SA 8000 et FDA, ils approvisionnent les bureaux d'approvisionnement des hôpitaux et les distributeurs médicaux en Amérique du Nord et en Europe.
- Type
- brand seeking distribution
- Location
- Sialkot, Pakistan
- Website
- drfrigz.com
- Categories
- Fournitures médicales et de santé
- Markets
- États-Unis, Allemagne, Royaume-Uni, France
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- certificate-page-on-site (amber), checked 2026-08-30 Company's own certification page
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- fda-registered (green), checked 2026-08-08 FDA
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 9001, Quality Management IAF CertSearch
- SA8000 Social Accountability SAAS certified facilities
- FDA Registered FDA Establishment Registration
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)