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Bal1-P3-20-35-200

EUDAMED

Class I (EU MDR)

Ref 70100166447

by FUJIFILM medwork GmbH

Identity

Trade Name
BAL1-P3-20-35-200 EUDAMED
Device Name
BAL1-Series EUDAMED
Model / Reference
70100166447 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503055583 EUDAMED
Basic UDI-DI
4044503056113U EUDAMED
EMDN Code
G03050101 DIGESTIVE ENDOSCOPY, RETRIEVAL BALLOON DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Bal1-P3-20-35-200 by FUJIFILM medwork GmbH — 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
DE-MF-000008444

Sources (1)

  • EUDAMED 7c9acaae-1bae-44f1-9db9-5a7074f71d18 61 fields · synced Jul 9, 2026