← Back to catalogue

Sf-H500

EUDAMED

Class IIb (EU MDR)

Ref -Model SF-H500

by Sonoscape Medical Corp.

Identity

Trade Name
SF-H500 EUDAMED
Device Name
Insufflator EUDAMED
Model / Reference
SF-H500 EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
06945868607661 EUDAMED
Basic UDI-DI
69458686SF-H500VJ EUDAMED
EMDN Code
Z12029008 GAS INFLATORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sf-H500 by Sonoscape Medical Corp. — Class IIb — 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-000009623
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED a6758e7d-6454-4374-acef-3b84025f043d 61 fields · synced Jun 18, 2026