Identity
- Trade Name
- Imaging and Pain Management FDA UDI
- Generic Name
- Fluoroscopy/angiography table, powered FDA UDI
- Device Name
- CFPM302 Integrated Top + Foot Control + 2” Table Top Pad + 5” Casters FDA UDI
- Model / Reference
- CFPM 302 FDA UDI
- Description
- CFPM302 Integrated Top + Foot Control + 2” Table Top Pad + 5” Casters FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817463026368 FDA UDI
- FDA Product Code
- IXR FDA UDI
- GMDN Term
- Fluoroscopy/angiography table, powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1980 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
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
Category: Fluoroscopy/angiography table, powered
Imaging and Pain Management by Oakworks, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Fluoroscopy/angiography table, powered.
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
- Oakworks, Inc.
Sources (1)
- FDA UDI eb97f217-9bc9-4d97-8e4c-90354462ab4d 33 fields · synced May 30, 2026