Identity
- Trade Name
- Mediblu FDA UDI
- Generic Name
- Foetal/maternal prenatal monitor FDA UDI
- Model / Reference
- FM02 FDA UDI
Identifiers
- Catalog Number
- MDB01008 FDA UDI
- Primary DI / UDI-DI
- B632MDB01008 FDA UDI
- 510(k) Number
- K102140 FDA UDI
- FDA Product Code
- HGM FDA UDI
- GMDN Term
- Foetal/maternal prenatal monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.2740 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Foetal/maternal prenatal monitor
Mediblu by Mediblu Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K102140 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
- Mediblu Medical, LLC
Sources (1)
- FDA UDI 168b27f8-a1db-42fa-aff4-ed33f21e8ee4 35 fields · synced Jun 8, 2026