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Bougie Dilator Sets

EUDAMED

Class IIa (EU MDR)

Ref HM302-18Model HM/302

by Changzhou Health Microport Medical Device Co., Ltd.

Identity

Trade Name
Bougie Dilator Sets EUDAMED
Device Name
Bougie Dilator Sets EUDAMED
Model / Reference
HM/302 EUDAMED
HM302-18 EUDAMED

Identifiers

Primary DI / UDI-DI
06951862291942 EUDAMED
Basic UDI-DI
B-06951862291942 EUDAMED
EMDN Code
G010101 OESOPHAGEAL BOUGIES EUDAMED
G010102 CARDIAS DILATATION TUBES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Bougie Dilator Sets by Changzhou Health Microport Medical Device 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-000033536
Authorised Representative
Llins Service & Consulting GmbH DE-AR-000009077

Sources (2)

  • EUDAMED 8d1efd21-1a17-46d2-979b-62fc8d9495be 61 fields · synced Jun 19, 2026
  • EUDAMED 69e77829-70e0-457b-a22f-226e3209636a 61 fields · synced Jun 14, 2026