Airos

FDA UDI

Class II (US FDA UDI)

by Airos Medical Inc

Identity

Trade Name: AIROS FDA UDI
Generic Name: Intermittent venous compression system FDA UDI
Device Name: ARTAIRA Arterial Compression Device FDA UDI
Model / Reference: AACD01 FDA UDI
Description: ARTAIRA Arterial Compression Device FDA UDI

Identifiers

Primary DI / UDI-DI: 00855682007379 FDA UDI
FDA Product Code: JOW FDA UDI
GMDN Term: Intermittent venous compression system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intermittent venous compression system

A comprehensive, noninvasive treatment and prevention system for venous disorders and sequelae. The AIROS device applies intermittent pressure to promote blood flow in the affected extremities.

Similar devices

Also classified as Intermittent venous compression system.

AIRCAST — DJO, LLC · Class II
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VenaOne, Pair of Batteries — Precision Medical Products · Class II
Movement and Compressions System (MAC) — Recovery Force, LLC · Class II
LX9max — DAESUNG MAREF CO., LTD. · Class II
Pulse Carry Case — NORMATEC INDUSTRIES, LP · Class II
Rapid Reboot Recovery Products — RAPID REBOOT RECOVERY PRODUCTS · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Airos Medical Inc

Sources (1)

FDA UDI 1b354151-eb50-45e7-966e-cdbd59ba8b17 35 fields · synced Jul 12, 2026