← Back to catalogue

Procare

FDA UDI

Class I (US FDA UDI)

by Djo, Llc

Identity

Trade Name
PROCARE FDA UDI
Generic Name
Wrist orthosis FDA UDI
Device Name
COMFORT FORM WRIST/THUMB,RT,M, OCCUPATIONAL MED OF COLUMBUS FDA UDI
Model / Reference
79-87305-4074 FDA UDI
Description
COMFORT FORM WRIST/THUMB,RT,M, OCCUPATIONAL MED OF COLUMBUS FDA UDI

Identifiers

Primary DI / UDI-DI
00190446135272 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Wrist orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wrist orthosis

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

Similar devices

Also classified as Wrist orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI b0222050-b948-4330-bc81-1c75c1b7c8e7 33 fields · synced May 31, 2026