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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

CAPIprotect — IVDR Class A IVDR by sebia

MD Atlas
sebia

EUDAMED last updated this device on Aug 4, 2022

CAPIprotect

3607362061BUBR

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: sebia
UDI-DI code: 03607360020616
Reference / catalog number: 2061

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Manufacturer information

Organization name: sebia
SRN: FR-MF-000003520
Manufacturer status: Active

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"AUTOMATIC LOW VOLUME" LABELS FOR MINICAP FLEX-PIERCING (20)3607369208BUF3On the market "MANUAL LOW VOLUME" LABELS FOR MINICAP FLEX-PIERCING (20)3607369209BUF8On the market 15 WELLS ANTISERA SEGMENT (10)3607364397BUF7On the market 18 WELLS ANTISERA SEGMENT (10)3607364398BUFCOn the market A1C/CE - CAPILLARY BLOOD SAMPLE KIT (A)3607369212BUECOn the market

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW007
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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: CAPIprotect
UDI-DI code: 03607360020616
Basic UDI-DI: 3607362061BUBR
Reference / catalog number: 2061
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Not applicable
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W01019099CLINICAL CHEMISTRY REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

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.