Identity
- Trade Name
- PHAKOS FDA UDI
- Generic Name
- Vitrectomy contact lens, single-use FDA UDI
- Device Name
- HR PANORAMIC wide angle lens, with ring and removable handle FDA UDI
- Model / Reference
- MV LV 48 HR FDA UDI
- Description
- HR PANORAMIC wide angle lens, with ring and removable handle FDA UDI
Identifiers
- Catalog Number
- MV LV 48 HR FDA UDI
- Primary DI / UDI-DI
- B564MVLV48HR0 FDA UDI
- FDA Product Code
- HJK FDA UDI
- GMDN Term
- Vitrectomy contact lens, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1385 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Category: Vitrectomy contact lens, single-use
Phakos by Phakos — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Vitrectomy contact lens, single-use — FCI S A S FCI 20 22 · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Phakos
Sources (1)
- FDA UDI db34c03c-1484-4708-8fd1-afebbc9850f3 34 fields · synced Jun 1, 2026