Identity
- Trade Name
- FetaLink® FDA UDI
- Generic Name
- Obstetrical monitoring/analysis software FDA UDI
- Model / Reference
- FetaLink2014 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00853023006043 FDA UDI
- 510(k) Number
- K091251 FDA UDI
- FDA Product Code
- HGM FDA UDI
- GMDN Term
- Obstetrical monitoring/analysis software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.2740 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
FetaLink® by Cerner Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K091251 also covers:
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
- Cerner Corporation
Sources (1)
- FDA UDI 4cc25314-b909-4aed-a57d-9ea164bff62b 34 fields · synced Jun 1, 2026