← Back to catalogue

Mylife Lancets

EUDAMED

Class IIa (EU MDR)

Ref 700023339Ref 700023340FOC 30G

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
Mylife Lancets EUDAMED
Device Name
Disposable Blood Lancets EUDAMED
Model / Reference
700023339 EUDAMED
700023340FOC 30G EUDAMED

Identifiers

Primary DI / UDI-DI
16945630115803 EUDAMED
16945630115810 EUDAMED
Basic UDI-DI
6945630101B9 EUDAMED
Unit of Use DI
06945630115806 EUDAMED
06945630115813 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Mylife Lancets by Sterilance Medical (Suzhou) Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000002860
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED a49180fb-8d30-4730-92cb-d40cadab5914 61 fields · synced Jul 19, 2026
  • EUDAMED 4f576ffd-d443-4d07-b076-6d65a167d901 61 fields · synced May 18, 2026