← Back to catalogue

Ez-Trax™

FDA UDI

Class II (US FDA UDI)

by K1 Medical Technologies, Llc

Identity

Trade Name
EZ-TRAX™ FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Divider (H) 2 x (L) 03 FDA UDI
Model / Reference
067.00 DIVIDER.2.03 FDA UDI
Description
Divider (H) 2 x (L) 03 FDA UDI

Identifiers

Catalog Number
067.00 DIVIDER.2.03 FDA UDI
Primary DI / UDI-DI
00850006159758 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

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: Instrument tray, reusable

Ez-Trax™ by K1 Medical Technologies, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, 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

Sources (1)

  • FDA UDI ef678cb0-d4af-4a6c-b821-bf6ab9254b76 34 fields · synced May 30, 2026