← Back to catalogue

Truliant

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name
Truliant FDA UDI
Generic Name
Surgical optical-tracking spatial marker, reusable FDA UDI
Model / Reference
02-521-90-0130 FDA UDI

Identifiers

Catalog Number
02-521-90-0130 FDA UDI
Primary DI / UDI-DI
10885862604903 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Surgical optical-tracking spatial marker, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

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: Surgical optical-tracking spatial marker, reusable

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

Similar devices

Also classified as Surgical optical-tracking spatial marker, 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 80b4c847-481e-4543-a4e9-51e17019a267 33 fields · synced Jun 8, 2026