Tools - WFS

FDA UDI

Class II (US FDA UDI)

by Trimed, INC.

Identity

Trade Name: Tools - WFS FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: WS3, Screw Caddy Block FDA UDI
Model / Reference: WS3-CADDY-BLOCK FDA UDI
Description: WS3, Screw Caddy Block FDA UDI

Identifiers

Catalog Number: WS3-CADDY-BLOCK FDA UDI
Primary DI / UDI-DI: 00842188128219 FDA UDI
510(k) Number: K243569 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Tools - WFS by Trimed, INC. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K243569 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Trimed, INC.

Sources (1)

FDA UDI 6c44b781-1536-4acc-b333-3d195405dc7e 36 fields · synced May 31, 2026