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Sterilization pouches

EUDAMED

Class I (EU MDR)

Ref 135 mm×250 mmModel Sterilization pouches

by Fomed Industries Inc.

Identity

Device Name
Sterilization pouches EUDAMED
Model / Reference
Sterilization pouches EUDAMED
135 mm×250 mm EUDAMED

Identifiers

Primary DI / UDI-DI
06973685040996 EUDAMED
Basic UDI-DI
697368504ZFDLN016W EUDAMED
EMDN Code
S01010101 STERILISATION POUCHES, FLAT, PAPER/PLASTIC FILM EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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 pouches by Fomed Industries Inc — 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-000012944
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 313bae5c-5b5c-48a4-b087-953fdb6f8a63 61 fields · synced Jul 13, 2026