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Aircast

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
AIRCAST FDA UDI
Generic Name
Circulating-fluid localized thermal therapy system control unit FDA UDI
Device Name
VENAPRO + ICEMAN CLASSIC CUBE FDA UDI
Model / Reference
30ICE FDA UDI
Description
VENAPRO + ICEMAN CLASSIC CUBE FDA UDI

Identifiers

Primary DI / UDI-DI
00190446293354 FDA UDI
FDA Product Code
JOW FDA UDI
ILO FDA UDI
GMDN Term
Circulating-fluid localized thermal therapy system control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
890.5720 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

Yes

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

No

FDA UDI

Category: Intermittent venous compression systemCirculating-fluid localized thermal therapy system control unit

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

Similar devices

Also classified as Circulating-fluid localized thermal therapy system control unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 7030921c-870a-447a-9325-ed9f786504ea 33 fields · synced May 29, 2026