Identity
- Trade Name
- Marc Hunter FDA UDI
- Generic Name
- Tinted non-prescription spectacle lens FDA UDI
- Device Name
- MH-7938 BLUE 54/19/145 FDA UDI
- Model / Reference
- MH7938-BLU-54 FDA UDI
- Description
- MH-7938 BLUE 54/19/145 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00754317205879 FDA UDI
- FDA Product Code
- HQY FDA UDI
- GMDN Term
- Tinted non-prescription spectacle lens FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.5850 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: Tinted non-prescription spectacle lens
A comprehensive 2-3 paragraph SEO description for the Marc Hunter medical device, written in clear and natural language.
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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
- New York Eye
Sources (1)
- FDA UDI dc1f1189-4bbc-4e1a-b5c5-b38a816f1f5d 33 fields · synced Jul 25, 2026