← Back to catalogue

Pro-Tech Pharma

EUDAMED

Class IIa (EU MDR)

Ref Soft 30G

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
PRO-TECH PHARMA EUDAMED
Device Name
Disposable Blood Lancets EUDAMED
Model / Reference
Soft 30G EUDAMED

Identifiers

Primary DI / UDI-DI
16945630137560 EUDAMED
Basic UDI-DI
6945630101B9 EUDAMED
Unit of Use DI
06945630137563 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Pro-Tech Pharma 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 (1)

  • EUDAMED 95afa622-9f69-4800-b165-3f09a7aa07ba 61 fields · synced Jul 19, 2026