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Biopsy Forceps, Spoon

EUDAMED

Class I (EU MDR)

Ref THF273541

by Joimax GmbH

Identity

Trade Name
Biopsy Forceps, Spoon EUDAMED
Device Name
Biopsy Forceps, Blakesley EUDAMED
Model / Reference
THF273541 EUDAMED

Identifiers

Primary DI / UDI-DI
04250337119616 EUDAMED
Basic UDI-DI
42503371FORCGRAG8 EUDAMED
Direct Marketing DI
04250337119616 EUDAMED
EMDN Code
L110602 NEUROSURGERY GRIPPERS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Flexible endoscopic biopsy forceps, reusable

Biopsy Forceps, Spoon by Joimax GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (1)

  • EUDAMED 68decce2-ee5d-46c4-b817-d7fde47b6e2e 61 fields · synced Jun 19, 2026