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Aadco

FDA UDI

Class I (US FDA UDI)

by Aadco Medical, Inc.

Identity

Trade Name
AADCO FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Device Name
POLY REPL ARM BOARD PDS FDA UDI
Model / Reference
P-182P FDA UDI
Description
POLY REPL ARM BOARD PDS FDA UDI

Identifiers

Catalog Number
P-182P FDA UDI
Primary DI / UDI-DI
00840348505955 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Arm procedure positioner, reusable

Aadco by Aadco Medical, Inc. — 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
Aadco Medical, Inc.

Sources (1)

  • FDA UDI 8d7ae23f-e01f-44a9-8838-014633c6dbf0 34 fields · synced May 30, 2026