Identity
- Trade Name
- Powerline Series Accessory FDA UDI
- Generic Name
- Radiology table extension FDA UDI
- Device Name
- 30" Powerline Table Extender Accessory FDA UDI
- Model / Reference
- 51910 FDA UDI
- Description
- 30" Powerline Table Extender Accessory FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817463027143 FDA UDI
- FDA Product Code
- LGX FDA UDI
- GMDN Term
- Radiology table extension FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4960 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: Radiology table extension
Powerline Series Accessory by Oakworks, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiology table extension.
- Powerline Acessory — OAKWORKS, INC. · Class I
- Ultrasound Product Line Accessory — OAKWORKS, INC. · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Oakworks, Inc.
Sources (1)
- FDA UDI 7bf03c9e-5402-47d8-aaac-a9e994a83f4d 33 fields · synced May 31, 2026