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Hydro Twister® Guidewire

EUDAMED

Class IIa (EU MDR)

Ref BHTN035150AT

by Blue Neem Medical Devices Private Limited

Identity

Trade Name
Hydro Twister® Guidewire EUDAMED
Device Name
Guidewire EUDAMED
Model / Reference
BHTN035150AT EUDAMED

Identifiers

Primary DI / UDI-DI
08905080072904 EUDAMED
Basic UDI-DI
8905080BUGW78 EUDAMED
EMDN Code
U0601 UROLOGICAL GUIDEWIRES, HYDROPHILIC 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

Hydro Twister® Guidewire by Blue Neem Medical Devices Private Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Manufacturer's product page: View Product >

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000021793
Authorised Representative
Arazy Group (Ireland) Ltd. IE-AR-000000093

Sources (1)

  • EUDAMED e853f3b5-4a95-4fa0-ae22-cb765e563346 61 fields · synced Oct 6, 2026