Identity
- Trade Name
- TF50 Trial Frame FDA UDI
- Generic Name
- Trial lens frame FDA UDI
- Model / Reference
- 15010 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00812559010559 FDA UDI
- FDA Product Code
- HPA FDA UDI
- GMDN Term
- Trial lens frame FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1415 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Trial lens frame
TF50 Trial Frame by Reichert Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Trial lens frame.
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- BK S1/T without convex cylinders, coated table version, trial lens case — OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung · Class I
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- Universal Trial Frame UB 4 — OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung · Class I
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
- Reichert Inc.
Sources (1)
- FDA UDI 88ef15ab-7072-487b-8b63-d7b5f3d45fbd 32 fields · synced May 30, 2026