Identity
- Trade Name
- SelectCells Mini FDA UDI
- Generic Name
- Endometrial biopsy kit FDA UDI
- Device Name
- Endometrial Sampling Device FDA UDI
- Model / Reference
- SM203 FDA UDI
- Description
- Endometrial Sampling Device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888937011227 FDA UDI
- 510(k) Number
- K954097 FDA UDI
- FDA Product Code
- HHK FDA UDI
- GMDN Term
- Endometrial biopsy kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.1175 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
SelectCells Mini by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 d8f0d29f-f860-4507-a8d0-987f1582fa5e 35 fields · synced Jun 9, 2026