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Anesthesia Armboard with 2" Pad

FDA UDI

Class I (US FDA UDI)

by Composite Manufacturing, Inc.

Identity

Trade Name
Anesthesia Armboard with 2" Pad FDA UDI
Generic Name
Armboard, reusable FDA UDI
Device Name
Carbon Fiber construction Armboard designed to integrate with surgical table side rail and support the patient arm for surgical procedures. FDA UDI
Model / Reference
1-1009-003 FDA UDI
Description
Carbon Fiber construction Armboard designed to integrate with surgical table side rail and support the patient arm for surgical procedures. FDA UDI

Identifiers

Primary DI / UDI-DI
00810105030280 FDA UDI
FDA Product Code
BWN FDA UDI
GMDN Term
Armboard, 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Armboard, reusable

Anesthesia Armboard with 2" Pad by Composite Manufacturing, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Armboard, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Composite Manufacturing, Inc.

Sources (1)

  • FDA UDI b729bc2b-77fd-42d2-9744-dd83a94addbc 34 fields · synced May 30, 2026