Dr. Frigz International
Sterile surgical instruments OEM/private-label producer with MDR-ready compliance.
Dr. Frigz produces a comprehensive range of sterile surgical, dental, and veterinary instruments under OEM and private-label arrangements. With ISO 13485, SA 8000, and FDA registration, they supply hospital procurement offices and medical distributors in North America and Europe.
- Type
- brand seeking distribution
- Location
- Sialkot, Pakistan
- Website
- drfrigz.com
- Categories
- Medical & Healthcare Supplies
- Markets
- United States, Germany, United Kingdom, 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)