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DePuy Synthes

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 291490005

by Tecomet, Inc

Identity

Trade Name
CROSSNAV Adaptor Modular Caddie EUDAMED
DePuy Synthes FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Surgical Instruments- Cases and Trays EUDAMED
CROSSNAV Adaptor Modular Caddie FDA UDI
Model / Reference
291490005 EUDAMEDFDA UDI
Description
CROSSNAV Adaptor Modular Caddie FDA UDI

Identifiers

Primary DI / UDI-DI
00817766026577 EUDAMEDFDA UDI
Basic UDI-DI
08177660213730Q6 EUDAMED
Direct Marketing DI
00817766026577 EUDAMED
FDA Product Code
KCT 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
Sterilization Method
Moist Heat or Steam Sterilization 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 e6828b5e-3503-45dd-b737-d5bbe1d4d030 33 fields · synced Sep 18, 2026
  • EUDAMED 864ffb71-470e-42b1-8a0d-3f59ea6927fb 61 fields · synced Jun 19, 2026