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mylife Softlance GD500 Lancing Devices

EUDAMED

Class I (EU MDR)

Ref 700023999Model GD500

by Bionime Corporation

Identity

Trade Name
mylife Softlance GD500 Lancing Devices EUDAMED
Device Name
Lancing Device EUDAMED
Model / Reference
GD500 EUDAMED
700023999 EUDAMED

Identifiers

Primary DI / UDI-DI
04710949332693 EUDAMED
Basic UDI-DI
471094933GD00001VG EUDAMED
Direct Marketing DI
04710949332693 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Category: Device sterilization/disinfection container, reusable

mylife Softlance GD500 Lancing Devices by Bionime Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Bionime Corporation
EUDAMED SRN
TW-MF-000008450
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED b2f03f56-78ff-4583-bc0b-f2b4ff07d9c3 61 fields · synced Jun 19, 2026