Identity
- Trade Name
- Ann Taylor FDA UDI
- Generic Name
- Tinted non-prescription spectacles FDA UDI
- Device Name
- SUNGLASSES -TYATP902 C02 TORT/BLUSH 51-15 130C FDA UDI
- Model / Reference
- TYATP90202 FDA UDI
- Description
- SUNGLASSES -TYATP902 C02 TORT/BLUSH 51-15 130C FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00882851359267 FDA UDI
- FDA Product Code
- HQY FDA UDI
- GMDN Term
- Tinted non-prescription spectacles 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
Yes
FDA UDI
Over-the-Counter
Yes
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 spectacles
A comprehensive directory of medical devices, showcasing the Ann Taylor Sunglasses (Non-Prescription Including Photosensitive) device.
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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
- L'Amy, Incorporated
Sources (1)
- FDA UDI a67ee739-04a7-46a6-a0bd-779cfcf7fd02 35 fields · synced Jun 29, 2026