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Sterilization Pouch

EUDAMED

Class I (EU MDR)

Ref AFD090260EModel AFD057130E,AFD070230E,AFD070260E,AFD090165E, AFD090230E,AFD090260E,AFD135260E,AFD135280E, AFD190360E,AFD305430E

by Anson Investment Development Co., Ltd.

Identity

Trade Name
Sterilization Pouch EUDAMED
Device Name
Sterilization Pouch EUDAMED
Model / Reference
AFD057130E,AFD070230E,AFD070260E,AFD090165E, AFD090230E,AFD090260E,AFD135260E,AFD135280E, AFD190360E,AFD305430E EUDAMED
AFD090260E EUDAMED

Identifiers

Primary DI / UDI-DI
06978049074105 EUDAMED
Basic UDI-DI
697804907AFDT3 EUDAMED
EMDN Code
S01010101 STERILISATION POUCHES, FLAT, PAPER/PLASTIC FILM EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Sterilization Pouch by Anson Investment Development Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000049926
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 8ff50e0d-1e11-4083-9181-ba5076e03705 61 fields · synced Aug 2, 2026