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Trimedyne® Omni™ Sterilization Tray System

FDA UDI

Class I (US FDA UDI)

by Trimedyne, Inc.

Identity

Trade Name
Trimedyne® Omni™ Sterilization Tray System FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
Omni Sterilization Tray System FDA UDI
Model / Reference
7205 FDA UDI
Description
Omni Sterilization Tray System FDA UDI

Identifiers

Catalog Number
7205 FDA UDI
Primary DI / UDI-DI
M47372050 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Surgical instrument interim-placement holder, 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical instrument interim-placement holder, reusable

Trimedyne® Omni™ Sterilization Tray System by Trimedyne, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trimedyne, Inc.

Sources (1)

  • FDA UDI 818e9ab8-5b9d-49d1-b70d-d46aad8e6058 35 fields · synced May 30, 2026