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Implant Container Hand

EUDAMEDFDA UDI

Class I (EU MDR)

Ref A-0890

by Medartis AG

Identity

Trade Name
Implant Container Hand EUDAMED
APTUS FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Container EUDAMED
Implant Container Hand FDA UDI
Model / Reference
A-0890 EUDAMEDFDA UDI
Description
Implant Container Hand FDA UDI

Identifiers

Catalog Number
A-0890 FDA UDI
Primary DI / UDI-DI
07630037852100 EUDAMEDFDA UDI
Basic UDI-DI
76300378000NY EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Device sterilization/disinfection container, reusable

Implant Container Hand by Medartis AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medartis AG
EUDAMED SRN
CH-MF-000022291
Authorised Representative
Medartis GmbH DE-AR-000005810

Sources (2)

  • EUDAMED 86e45919-e7d3-44ad-bc3b-091ee6656e1f 61 fields · synced Jul 21, 2026
  • FDA UDI 8555f3a7-32ac-4deb-8424-3580d705e85c 34 fields · synced May 30, 2026