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SiKo/Endo 290/080/052 oR oG DS mD 2-fach

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 7500831Model Siebkörbe

by Hupfer Metallwerke GmbH & Co KG

Identity

Trade Name
SiKo/Endo 290/080/052 oR oG DS mD 2-fach EUDAMED
Endoscope container with lid, stainless FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
steel, e-polished, for 2 endoscopes 290x80x52 mm FDA UDI
Model / Reference
Siebkörbe EUDAMED
7500831 EUDAMED
80-690-02 FDA UDI
Description
steel, e-polished, for 2 endoscopes 290x80x52 mm FDA UDI

Identifiers

Catalog Number
80-690-02 FDA UDI
Primary DI / UDI-DI
04044593003747 EUDAMEDFDA UDI
Basic UDI-DI
4044593SiebkoerbeNU EUDAMED
Direct Marketing DI
04044593003747 EUDAMED
FDA Product Code
MMO 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 EUDAMEDFDA UDI
Regulation Number
874.4420 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument tray, reusable

SiKo/Endo 290/080/052 oR oG DS mD 2-fach by Hupfer Metallwerke GmbH & Co KG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000007652

Sources (2)

  • EUDAMED 3b0df2e3-df36-4030-beb5-e5ca077368b8 61 fields · synced Oct 7, 2026
  • FDA UDI b27c70c5-9e67-4499-b905-097983d06775 35 fields · synced May 30, 2026