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DePuy Synthes

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 854793

by Tecomet, Inc

Identity

Trade Name
Thoracolumbar Lid for Instruments Tray 2 Stainless Steel EUDAMED
DePuy Synthes FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Surgical Instruments- Cases and Trays EUDAMED
Thoracolumbar Lid for Instruments Tray 2 Stainless Steel FDA UDI
Model / Reference
854793 EUDAMED
Thoracolumbar Lid for Instruments Tray 2 FDA UDI
Description
Thoracolumbar Lid for Instruments Tray 2 Stainless Steel FDA UDI

Identifiers

Catalog Number
854793 FDA UDI
Primary DI / UDI-DI
00817766025471 EUDAMEDFDA UDI
Basic UDI-DI
08177660213730Q6 EUDAMED
Direct Marketing DI
00817766025471 EUDAMED
FDA Product Code
FRG FDA UDI
EMDN Code
S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Category: Device sterilization/disinfection container, reusable

DePuy Synthes by Tecomet, Inc — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tecomet, Inc

Sources (2)

  • FDA UDI a447cdd3-08da-4508-8b3e-9424616dcb8a 34 fields · synced Sep 18, 2026
  • EUDAMED e728982e-6a0a-4463-98ec-f9da641d8169 61 fields · synced Jun 18, 2026