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mylife AutoLance GD720 Lancing Devices

EUDAMED

Class I (EU MDR)

Ref 700023995Model GD720

by Bionime Corporation

Identity

Trade Name
mylife AutoLance GD720 Lancing Devices EUDAMED
Device Name
Lancing Device EUDAMED
Model / Reference
GD720 EUDAMED
700023995 EUDAMED

Identifiers

Primary DI / UDI-DI
04710949333034 EUDAMED
Basic UDI-DI
471094933GD00002VJ EUDAMED
Direct Marketing DI
04710949333034 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

mylife AutoLance GD720 Lancing Devices by Bionime Corporation — 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

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

Sources (1)

  • EUDAMED 17ac5930-2d8b-4250-97e2-59c5a97b346e 61 fields · synced Jun 18, 2026