Identity
- Trade Name
- TRUMPF MEDICAL FDA UDI
- Generic Name
- Operating table patient pressure distribution pad, reusable FDA UDI
- Device Name
- Pad OR tabletop MR Neuro FDA UDI
- Model / Reference
- 2064890 FDA UDI
- Description
- Pad OR tabletop MR Neuro FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00887761994737 FDA UDI
- FDA Product Code
- JEA FDA UDIKXJ FDA UDI
- GMDN Term
- Operating table patient pressure distribution pad, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 FDA UDI892.1980 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
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Safe FDA UDI
Trumpf Medical by Baxter Medical Systems GmbH + Co. KG — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Baxter Medical Systems GmbH + Co. KG
Sources (1)
- FDA UDI 7253e0bb-0969-40d9-9240-c8d8770ad3c2 35 fields · synced Jun 6, 2026