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Aircast

FDA UDI

Class I (US FDA UDI)

by Djo, Llc

Identity

Trade Name
AIRCAST FDA UDI
Generic Name
Multi-chamber venous compression system garment, reusable FDA UDI
Device Name
VENAPRO SLEEVE EXTENDER FDA UDI
Model / Reference
3111-020 FDA UDI
Description
VENAPRO SLEEVE EXTENDER FDA UDI

Identifiers

Primary DI / UDI-DI
00888912308281 FDA UDI
FDA Product Code
IOD FDA UDI
GMDN Term
Multi-chamber venous compression system garment, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5350 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-chamber venous compression system garment, reusable

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

Similar devices

Also classified as Multi-chamber venous compression system garment, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI e3a73d30-3c95-49ed-a7d6-268bf916701b 33 fields · synced May 30, 2026