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Hydrus

EUDAMED

Class IIa (EU MDR)

Ref 02Model PB-020-300-090

by Skynor Medical(Shanghai)Co., Ltd

Identity

Trade Name
Hydrus EUDAMED
Device Name
Balloon Dilatation Catheter EUDAMED
Model / Reference
PB-020-300-090 EUDAMED
02 EUDAMED

Identifiers

Primary DI / UDI-DI
06970757204638 EUDAMED
Basic UDI-DI
B-06970757204638 EUDAMED
EMDN Code
C01050299 INTRAVASCULAR EMBOLIC PROTECTION CATHETERS AND SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Hydrus by Skynor Medical(Shanghai)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

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Manufacturer

EUDAMED SRN
CN-MF-000028227
Authorised Representative
Kingsmead Service B.V. NL-AR-000002066

Sources (1)

  • EUDAMED 6571dbfc-a607-49bf-aab3-7fd5ed33cffa 61 fields · synced Jun 18, 2026