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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

BHAU — Class I MDR by BMB MEDICAL

MD Atlas
BMB MEDICAL

EUDAMED last updated this device on Dec 21, 2023

BHAU

376034596BHAUCT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BMB MEDICAL
UDI-DI code: 37603459602296
Reference / catalog number: BHAU

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Manufacturer information

Organization name: BMB MEDICAL
SRN: FR-MF-000011270
Manufacturer status: —

Related devices

CARVI 60CM376034596CRCO6BSOn the market CARVI 70CM376034596CRCO6BSOn the market CARVI 80CM376034596CRCO6BSOn the market CLAVIA FCD 65376034596FCD7BDOn the market CLAVIA FCD 75376034596FCD7BDOn the market

Market distribution

Primary placement in Austria; available across 1 country total.

Placed on the market in Austria; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 37603459602296
Basic UDI-DI: 376034596BHAUCT
Reference / catalog number: BHAU
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050103EMERGENCY AND TRAUMATOLOGY STRETCHERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.