← Back to catalogue

Tools - EFS

FDA UDI

Class I (US FDA UDI)

by Trimed, INC.

Identity

Trade Name
Tools - EFS FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Elbow Forearm Screw Caddy FDA UDI
Model / Reference
EFS-SCREW FDA UDI
Description
Elbow Forearm Screw Caddy FDA UDI

Identifiers

Catalog Number
EFS-SCREW FDA UDI
Primary DI / UDI-DI
00842188110818 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

Tools - EFS by Trimed, INC. — Class I — 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

Manufacturer
Trimed, INC.

Sources (1)

  • FDA UDI ec4239ef-0263-49f9-b6ea-51313d84213a 35 fields · synced May 31, 2026