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Trainers Choice

FDA UDI

Class I (US FDA UDI)

by Trainer's Choice Inc

Identity

Trade Name
TRAINERS CHOICE FDA UDI
Generic Name
Knee support orthosis FDA UDI
Device Name
PATELLAR SLEEVE LG FDA UDI
Model / Reference
102 FDA UDI
Description
PATELLAR SLEEVE LG FDA UDI

Identifiers

Primary DI / UDI-DI
00831313000100 FDA UDI
FDA Product Code
ITQ FDA UDI
GMDN Term
Knee support 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

Yes

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: Knee support orthosis

Trainers Choice by Trainer's Choice Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee support orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e0fda710-ce0d-46d8-8e57-3c6290eeccf6 34 fields · synced May 30, 2026