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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

CKCO — Class I MDR by BMB MEDICAL

MD Atlas
BMB MEDICAL

EUDAMED last updated this device on Dec 21, 2023

CKCO

376034596CKCODB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BMB MEDICAL
UDI-DI code: 37603459603668
Reference / catalog number: CKCO

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Manufacturer information

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

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 37603459603668
Basic UDI-DI: 376034596CKCODB
Reference / catalog number: CKCO
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)

V08050199PATIENT TRANSFER STRETCHERS - OTHER

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

Related devices

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

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.