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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
Arm procedure positioner, reusable FDA UDI
Device Name
1” DLX ARMBOARD PAD, 1"T x 6"W x 26"L FDA UDI
Model / Reference
AP126-PR FDA UDI
Description
1” DLX ARMBOARD PAD, 1"T x 6"W x 26"L FDA UDI

Identifiers

Catalog Number
AP126-PR FDA UDI
Primary DI / UDI-DI
10810087352827 FDA UDI
FDA Product Code
LWG FDA UDI
GMDN Term
Arm procedure positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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: Arm procedure positioner, reusable

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

Similar devices

Also classified as Arm procedure positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 268513a1-382d-4082-b1ab-fd801620d9bb 34 fields · synced Jun 1, 2026