Identity
- Trade Name
- Bellinger FDA UDI
- Generic Name
- Spectacle frame FDA UDI
- Device Name
- Spectacle frame FDA UDI
- Model / Reference
- VENOM-246 FDA UDI
- Description
- Spectacle frame FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05712544163985 FDA UDI
- FDA Product Code
- HQZ FDA UDI
- GMDN Term
- Spectacle frame FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5842 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Spectacle frame
A comprehensive device review and comparison for the Bellinger Spectacle Frame, including its features, compliance status, and FAQs.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Bellinger A/S
Sources (1)
- FDA UDI 916673b0-18d4-4afa-872f-c0d3ba268a84 33 fields · synced Jul 18, 2026