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Silicone tip

EUDAMED

Class I (EU MDR)

Ref HG-ST02Model HG-ST01, HG-ST02, HG-ST03, HG-ST04, HG-ST05, HG-ST06, HG-ST07, HG-ST08, HG-ST09, HG-ST10Model HG-ST01,HG-ST02,HG-ST03,HG-ST04,HG-ST05,HG-ST06,HG-ST07,HG-ST08,HG-ST09,HG-ST10

by Hangzhou Weize Imp & Exp Co., Ltd.

Identity

Device Name
Silicone tip EUDAMED
Model / Reference
HG-ST01, HG-ST02, HG-ST03, HG-ST04, HG-ST05, HG-ST06, HG-ST07, HG-ST08, HG-ST09, HG-ST10 EUDAMED
HG-ST02 EUDAMED
HG-ST01,HG-ST02,HG-ST03,HG-ST04,HG-ST05,HG-ST06,HG-ST07,HG-ST08,HG-ST09,HG-ST10 EUDAMED

Identifiers

Primary DI / UDI-DI
06976543671417 EUDAMED
Basic UDI-DI
697654367SiliconetipLS EUDAMED
EMDN Code
Q030199 NASOPHARYNGEAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMEDEUDAMED

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

Silicone tip by Hangzhou Weize Imp & Exp Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000036544
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED d663cd7a-90bf-4e5e-988f-d175076fdfc8 61 fields · synced Jun 19, 2026
  • EUDAMED f140484e-c318-4421-930b-93f236208719 61 fields · synced Jun 19, 2026