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Coulmed

FDA UDI

Class I (US FDA UDI)

by Coulmed Products Group Llc

Identity

Trade Name
Coulmed FDA UDI
Generic Name
Operating table patient positioning set, reusable FDA UDI
Device Name
Armboard Pad, Gel and Pressure Relief Memory Foam Combo, 2"T x 6"W x 26"L..(Old Item #GP298-2) FDA UDI
Model / Reference
AP226-GPR FDA UDI
Description
Armboard Pad, Gel and Pressure Relief Memory Foam Combo, 2"T x 6"W x 26"L..(Old Item #GP298-2) FDA UDI

Identifiers

Catalog Number
AP226-GPR FDA UDI
Primary DI / UDI-DI
10810087350878 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Operating table patient positioning set, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Operating table patient positioning set, reusable

Coulmed by Coulmed Products Group Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating table patient positioning set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6a46aa60-67c3-4ca9-9b69-ae9b1c5a75b8 34 fields · synced May 31, 2026