Identity
- Trade Name
- KSK 150 FC FDA UDI
- Generic Name
- Colposcope FDA UDI
- Model / Reference
- 302303-0000-000 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04049539060228 FDA UDI
- FDA Product Code
- HEX FDA UDI
- GMDN Term
- Colposcope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1630 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Colposcope
Ksk 150 Fc by Carl Zeiss Meditec AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Colposcope.
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- Henry Schein — HENRY SCHEIN, INC. · Class II
- MICROSTAR Colposcope — Ecleris · Class II
- Gynex — GYNEX CORPORATION · Class II
- MICROSCOPE Colposcope — Ecleris · Class II
- WALLACH — CooperSurgical, Inc. · Class II
- Henry Schein — HENRY SCHEIN, 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 |
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Manufacturer
- Manufacturer
- Carl Zeiss Meditec AG
Sources (1)
- FDA UDI 312e6bb9-f746-4779-aa5b-e489659994eb 32 fields · synced May 30, 2026