Identity
- Trade Name
- WALLACH FDA UDI
- Generic Name
- Colposcope FDA UDI
- Device Name
- WALLACH® USB Video Conversion Kit FDA UDI
- Model / Reference
- 906170 FDA UDI
- Description
- WALLACH® USB Video Conversion Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937013740 FDA UDI
- 510(k) Number
- K853389 FDA UDI
- FDA Product Code
- DRC FDA UDI
- GMDN Term
- Colposcope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1390 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Colposcope
Wallach by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Colposcope.
- MICROSCOPE Colposcope — Ecleris · Class II
- Bovie — BOVIE MEDICAL CORPORATION · Class II
- Henry Schein — HENRY SCHEIN, INC. · Class II
- MICROSTAR Colposcope — Ecleris · Class II
- Gynex — GYNEX CORPORATION · Class II
- MICROSCOPE Colposcope — Ecleris · Class II
- Henry Schein — HENRY SCHEIN, INC. · Class II
- Galileo Colposcope, Direct Access — GYNEX CORPORATION · Class II
Cleared under the same submission
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 9cc48e35-ddfa-40bb-ae0e-b49275b4c4a4 34 fields · synced Jun 9, 2026