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Spe1-B5-21-120

EUDAMED

Class I (EU MDR)

Ref 70100146822Model SPE1-B5-21-120

by FUJIFILM medwork GmbH

Identity

Trade Name
SPE1-B5-21-120 EUDAMED
Device Name
SPE1-B5-Series EUDAMED
Model / Reference
SPE1-B5-21-120 EUDAMED
70100146822 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503020918 EUDAMED
Basic UDI-DI
B-04044503020918 EUDAMED
EMDN Code
R070299 BRONCHOSCOPIC SURGERY INSTRUMENTS, SINGLE-USE - OTHER 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

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Spe1-B5-21-120 by FUJIFILM medwork GmbH — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000008444

Sources (1)

  • EUDAMED 9819a848-d9f3-4a07-89e7-4dc508bdadbf 61 fields · synced Jun 18, 2026