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Mission Safety Lancets Ⅲ

EUDAMED

Class IIa (EU MDR)

Ref C121-3101

by Acon Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
Mission Safety Lancets Ⅲ EUDAMED
Device Name
Mission Safety Lancets Ⅲ EUDAMED
Model / Reference
C121-3101 EUDAMED

Identifiers

Primary DI / UDI-DI
D-C121-3101RL EUDAMED
Basic UDI-DI
B-C121-3101RL EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Blood lancet, single-use

Mission Safety Lancets Ⅲ by Acon Biotech (Hangzhou) Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000006977
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 552299f8-dc19-45ab-a2a9-473cbef9ab23 61 fields · synced Aug 1, 2026