Oakworks Medical

FDA UDI

Class II (US FDA UDI)

by Oakworks, Inc.

Identity

Trade Name: Oakworks Medical FDA UDI
Generic Name: Radiological general body-part positioner FDA UDI
Device Name: CFPM301 with 5" casters + Non-USA electr. FDA UDI
Model / Reference: CFPM301 FDA UDI
Description: CFPM301 with 5" casters + Non-USA electr. FDA UDI

Identifiers

Primary DI / UDI-DI: 00817463020472 FDA UDI
FDA Product Code: IXR FDA UDI
GMDN Term: Radiological general body-part positioner 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiological general body-part positioner

Oakworks Medical by Oakworks, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological general body-part positioner.

AADCO — AADCO MEDICAL, INC. · Class I
Techno-Aide — TECHNO-AIDE, INC. · Class I
Techno-Aide — TECHNO-AIDE, INC. · Class I
Techno-Aide — TECHNO-AIDE, INC. · Class I
pearltec — Pearl Technology AG · Class I
AADCO — AADCO MEDICAL, INC. · Class I
FoamFit Wedge 18x11x5 — Pearl Technology AG · Class I
AADCO — AADCO MEDICAL, 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 II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Oakworks, Inc.

Sources (1)

FDA UDI 6830ca63-b0af-4cf6-a3bc-12786d961f8b 33 fields · synced May 30, 2026