Identity
- Trade Name
- Pads FDA UDI
- Generic Name
- Operating table patient pressure distribution pad, reusable FDA UDI
- Device Name
- Pad upper back section B FDA UDI
- Model / Reference
- 1851978 FDA UDI
- Description
- Pad upper back section B FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00887761969582 FDA UDI
- FDA Product Code
- KXJ FDA UDIGDC FDA UDIJEA FDA UDI
- GMDN Term
- Operating table patient pressure distribution pad, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1980 FDA UDI878.4960 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
Pads by Baxter Medical Systems GmbH + Co. KG — 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 |
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Manufacturer
- Manufacturer
- Baxter Medical Systems GmbH + Co. KG
Sources (1)
- FDA UDI 30b9ad05-c29e-41ec-add6-c5a9bd5772a7 35 fields · synced Jun 1, 2026