Identity
- Trade Name
- Sentimag FDA UDI
- Generic Name
- Magnetic metal detector FDA UDI
- Device Name
- Sentimag Gen 3 Base Unit FDA UDI
- Model / Reference
- Gen 3 FDA UDI
- Description
- Sentimag Gen 3 Base Unit FDA UDI
Identifiers
- Catalog Number
- SMB03 FDA UDI
- Primary DI / UDI-DI
- 15060391210312 FDA UDI
- FDA Product Code
- NEU FDA UDIPUV FDA UDI
- GMDN Term
- Magnetic metal detector FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4300 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
No
FDA UDI
MR Unsafe FDA UDI
Category: Magnetic metal detector
Sentimag by Endomagnetics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Endomagnetics Ltd
Sources (1)
- FDA UDI 225de6d6-30a6-4bc7-8d60-1d1cc0f3dfad 34 fields · synced Jun 8, 2026