Identity
- Trade Name
- Trichiasis FDA UDI
- Generic Name
- Cryogenic analgesia unit FDA UDI
- Device Name
- Trichiasis, 3 mm Multi-Lash Probe FDA UDI
- Model / Reference
- DM172 FDA UDI
- Description
- Trichiasis, 3 mm Multi-Lash Probe FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937019896 FDA UDI
- FDA Product Code
- HQA FDA UDI
- GMDN Term
- Cryogenic analgesia unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4170 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
No
FDA UDI
Category: Cryogenic analgesia unit
Trichiasis by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cryogenic analgesia unit.
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC. · Class II
- Epimed — EPIMED INTERNATIONAL, INC · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- CooperSurgical, Inc.
Sources (1)
- FDA UDI 26355d5f-ec25-4922-9f12-22fac776d058 33 fields · synced Jun 9, 2026