Identity
- Trade Name
- Rovers® Cervex-Brush® Combi FDA UDI
- Generic Name
- Cytology scraper, single-use FDA UDI
- Device Name
- Cervical cell sampler FDA UDI
- Model / Reference
- 380101000 FDA UDI
- Description
- Cervical cell sampler FDA UDI
Identifiers
- Primary DI / UDI-DI
- 87191892460702 FDA UDI
- 510(k) Number
- K043369 FDA UDI
- FDA Product Code
- HHT FDA UDI
- GMDN Term
- Cytology scraper, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4530 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Rovers® Cervex-Brush® Combi by Rovers Medical Devices B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
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Manufacturer
- Manufacturer
- Rovers Medical Devices B.V.
Sources (1)
- FDA UDI da5951df-3a81-4986-89e8-110d9a3a8b77 36 fields · synced May 30, 2026