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Compex

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
COMPEX FDA UDI
Generic Name
Elbow orthosis FDA UDI
Device Name
COMPEX LT FDA UDI
Model / Reference
CX182WI04 FDA UDI
Description
COMPEX LT FDA UDI

Identifiers

Primary DI / UDI-DI
00190446303183 FDA UDI
FDA Product Code
GZI FDA UDI
GMDN Term
Elbow orthosis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Elbow orthosis

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

Similar devices

Also classified as Elbow orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI db3c3c42-3ab3-4b2e-bace-e09b69985ee0 33 fields · synced May 31, 2026