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HandX Fenestrated Grasper

EUDAMED

Class IIa (EU MDR)

Ref 20-30-013-02Model 20-30-011-02

by HumanTouch Surgical LTD.

Identity

Trade Name
HandX Fenestrated Grasper EUDAMED
Device Name
HandX Needle Holder EUDAMED
Model / Reference
20-30-011-02 EUDAMED
20-30-013-02 EUDAMED

Identifiers

Primary DI / UDI-DI
07290017376073 EUDAMED
Basic UDI-DI
07290017376HXP001WG EUDAMED
EMDN Code
K01020104 MINIMALLY INVASIVE SURGERY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

HandX Fenestrated Grasper by HumanTouch Surgical LTD. — Class IIa — 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
IL-MF-000009116
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (1)

  • EUDAMED 18fa453e-8c5e-4ea6-b09c-174359b620bf 61 fields · synced Jul 10, 2026