← Back to catalogue

Truliant

FDA UDI

Class I (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Truliant FDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
TRIAL, CRC TIBIAL INSERT, SIZE 4.5 FDA UDI
Model / Reference
02-029-25-3445 FDA UDI
Description
TRIAL, CRC TIBIAL INSERT, SIZE 4.5 FDA UDI

Identifiers

Catalog Number
02-029-25-3445 FDA UDI
Primary DI / UDI-DI
10885862556653 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Knee tibia prosthesis trial, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 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

Yes

FDA UDI

Over-the-Counter

No

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Knee tibia prosthesis trial, reusable

Truliant by Exactech, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee tibia prosthesis trial, reusable.

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
Exactech, Inc.

Sources (1)

  • FDA UDI cc8913d4-58d7-4b6b-93f0-78855d51cc50 35 fields · synced May 30, 2026