Bm-Bid-II30B

by BrosMed Medical Co., Ltd

Ref BM-BID-II30BModel Balloon Inflation Device Sets

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number695848140030LY Basic UDI-DI 06958481431124UDI-DI	Date5 Jun 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference: Balloon Inflation Device Sets, BM-BID-II30B

Primary DI / UDI-DI: 06958481431124
Basic UDI-DI: 695848140030LY
EMDN Code: C0699 Cardiovascular surgery instruments, single-use - other

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: CN-MF-000007501
Authorised representative: Brosmed Medical B.V. NL-AR-000002616

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Properties

Sterile

Other properties (12)

Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No