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Pad Armboard Universal

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
PAD ARMBOARD UNIVERSAL FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Model / Reference
924928 FDA UDI

Identifiers

Catalog Number
2970012405 FDA UDI
Primary DI / UDI-DI
00733657238624 FDA UDI
FDA Product Code
BWN 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

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Arm procedure positioner, reusable

Pad Armboard Universal by AliMed, 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

Manufacturer
AliMed, LLC

Sources (1)

  • FDA UDI 102a0775-c9a9-407d-8e7f-9e2309adc0c6 34 fields · synced Jun 9, 2026