Identity
- Trade Name
- Portable DR Panel Protector FDA UDI
- Generic Name
- Computed radiography digital imaging scanner FDA UDI
- Device Name
- Radiologic table FDA UDI
- Model / Reference
- 9890-010-88161 FDA UDI
- Description
- Radiologic table FDA UDI
Identifiers
- Catalog Number
- 712031 FDA UDI
- Primary DI / UDI-DI
- 00884838074286 FDA UDI
- FDA Product Code
- KXJ FDA UDI
- GMDN Term
- Computed radiography digital imaging scanner FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1980 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
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
No
FDA UDI
Portable DR Panel Protector by Philips Medical Systems GmbH, Dmc — 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
- Philips Medical Systems GmbH, Dmc
Sources (1)
- FDA UDI 6a16bf2b-de2f-4a4b-9d5d-7de1dc1f5e5e 35 fields · synced May 31, 2026