Identity
- Trade Name
- Magnification Lens EUDAMEDFDA UDI
- Generic Name
- ENT instrument magnifying lens FDA UDI
- Device Name
- Magnification Lens EUDAMEDFDA UDI
- Model / Reference
- 2265 EUDAMEDFDA UDI
- Description
- Magnification Lens FDA UDI
Identifiers
- Catalog Number
- 2265 FDA UDI
- Primary DI / UDI-DI
- 00859911004757 EUDAMEDFDA UDI
- Basic UDI-DI
- 859911004MagLensMS EUDAMED
- Unit of Use DI
- 10859911004754 EUDAMED
- FDA Product Code
- JYG FDA UDI
- EMDN Code
- Z12149080 VARIOUS ENT INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- ENT instrument magnifying lens FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 874.4420 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Magnification Lens by Bionix, LLC — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 859911004MagLensMS | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Bionix LLC
- EUDAMED SRN
- US-MF-000020408
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (2)
- EUDAMED 7502afe3-d25b-49f0-b83a-8b9b186658fd 61 fields · synced Aug 4, 2026
- FDA UDI 263044d8-62de-46cf-8e3d-f6185a363010 35 fields · synced May 30, 2026