Identity
- Trade Name
- Walcott Rx Products FDA UDI
- Generic Name
- Flieringa ophthalmic ring FDA UDI
- Device Name
- Flieringa Ring FDA UDI
- Model / Reference
- Rx181-22 FDA UDI
- Description
- Flieringa Ring FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840285313590 FDA UDI
- FDA Product Code
- HJB FDA UDI
- GMDN Term
- Flieringa ophthalmic ring FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.1450 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Flieringa ophthalmic ring
Walcott Rx Products by Walcott Rx Product Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flieringa ophthalmic ring.
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- MR PHACO — Crestpoint Management Ltd. · Class I
- Symmetry Flieringa — SYMMETRY SURGICAL INC. · Class I
- MR PHACO — Crestpoint Management Ltd. · Class I
- V. Mueller — STERIS CORPORATION · 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
- Walcott Rx Product Inc
Sources (1)
- FDA UDI 5b1a7210-2f5f-42ba-be08-e0ce67f99d13 34 fields · synced May 30, 2026