← Back to catalogue

Balloon Inflation Device Sets

EUDAMED

Class I (EU MDR)

Ref BR-BID-III30F

by Brun Medical Co., Ltd.

Identity

Device Name
Balloon Inflation Device Sets EUDAMED
Model / Reference
BR-BID-III30F EUDAMED

Identifiers

Primary DI / UDI-DI
06973245041418 EUDAMED
Basic UDI-DI
697324504BIDS0017PH EUDAMED
EMDN Code
C0699 CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Balloon Inflation Device Sets by Brun Medical 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000009738
Authorised Representative
Cnovate Medical B.V. NL-AR-000039205

Sources (1)

  • EUDAMED b8ac8659-b96a-4be4-bb56-a78d2593b4b7 61 fields · synced Jun 18, 2026