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Procare

FDA UDI

Class I (US FDA UDI)

by Djo, Llc

Identity

Trade Name
PROCARE FDA UDI
Generic Name
Abdominal binder, reusable FDA UDI
Device Name
BINDER, ABD 4PNL 12 IN 45 IN - 62 IN UNSX FDA UDI
Model / Reference
155-79-89091 FDA UDI
Description
BINDER, ABD 4PNL 12 IN 45 IN - 62 IN UNSX FDA UDI

Identifiers

Primary DI / UDI-DI
00190446660279 FDA UDI
FDA Product Code
FSD FDA UDI
GMDN Term
Abdominal binder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5160 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

Yes

FDA UDI

Category: Abdominal binder, reusable

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

Similar devices

Also classified as Abdominal binder, 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 312658b9-8014-493c-84cf-23b7309f8466 33 fields · synced May 30, 2026