← Back to catalogue

Surpass

EUDAMED

Class IIa (EU MDR)

Ref SSGW-35-260

by Lifetech Scientific (Shenzhen) Co., Ltd.

Identity

Trade Name
Surpass EUDAMED
Device Name
Surpass™ Super Stiff Guidewire EUDAMED
Model / Reference
SSGW-35-260 EUDAMED

Identifiers

Primary DI / UDI-DI
06938370135074 EUDAMED
Basic UDI-DI
B-06938370135074 EUDAMED
EMDN Code
C04020202 PERIPHERAL VASCULAR THERAPEUTIC GUIDEWIRES, NON-HYDROPHILIC 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

Surpass by Lifetech Scientific (Shenzhen) Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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

Manufacturer

EUDAMED SRN
CN-MF-000001561
Authorised Representative
LifeTech Scientific (Europe) B.V. NL-AR-000000804

Sources (1)

  • EUDAMED 8e57870f-0fe7-4e62-bac9-548c902a1068 61 fields · synced Oct 6, 2026