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Aircast

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
AIRCAST FDA UDI
Generic Name
Intermittent venous compression system FDA UDI
Device Name
TUBE ASSY, VENAFLOW ELITE, STD FDA UDI
Model / Reference
3008 FDA UDI
Description
TUBE ASSY, VENAFLOW ELITE, STD FDA UDI

Identifiers

Primary DI / UDI-DI
00888912022248 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intermittent venous compression system

Aircast by Djo, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent venous compression system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 66737ae1-46ee-4ce8-bf30-4aa58e38b411 33 fields · synced Jun 1, 2026