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TracPatch

FDA UDI

Class I (US FDA UDI)

by Tracpatch Health, LLC

Identity

Trade Name
TracPatch FDA UDI
Generic Name
Electronic goniometer/kinesiology sensor FDA UDI
Device Name
Knee System FDA UDI
Model / Reference
4000-0-1000 FDA UDI
Description
Knee System FDA UDI

Identifiers

Catalog Number
4000-0-1000 FDA UDI
Primary DI / UDI-DI
00844588044311 FDA UDI
FDA Product Code
KQX FDA UDI
GMDN Term
Electronic goniometer/kinesiology sensor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electronic goniometer/kinesiology sensor

TracPatch by Tracpatch Health, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic goniometer/kinesiology sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5aec659d-1127-4b00-817e-43c80f69603d 35 fields · synced Jun 6, 2026