← Back to catalogue

Inhalation Antalgic Equipment(Sedation system)

EUDAMED

Class IIa (EU MDR)

Ref AII5000F

by Ambulanc(Shenzhen)Tech.Co., Ltd.

Identity

Trade Name
Inhalation Antalgic Equipment(Sedation system) EUDAMED
Device Name
Inhalation Antalgic Equipment(Sedation system) EUDAMED
Model / Reference
AII5000F EUDAMED

Identifiers

Primary DI / UDI-DI
06970658140547 EUDAMED
Basic UDI-DI
B-06970658140547 EUDAMED
EMDN Code
R060203 INHALATION THERAPY HUMIDIFICATION LIQUIDS EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

No

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

Inhalation Antalgic Equipment(Sedation system) by Ambulanc(Shenzhen)Tech.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-000010435
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 0458e383-2bff-4f40-af81-55599e77d56c 61 fields · synced Jun 19, 2026