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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

Digest-EUR — IVDR Class A IVDR by Eurobio Scientific

MD Atlas
Eurobio Scientific

EUDAMED last updated this device on Nov 2, 2022

Digest-EUR

3661605DD0DIG00B6

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Eurobio Scientific
UDI-DI code: 03366160500260
Reference / catalog number: DD0DIG00-AI

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Manufacturer information

Organization name: Eurobio Scientific
SRN: FR-MF-000011745
Manufacturer status: Active

Critical warnings

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

CW073
EUDAMED did not publish a description for this code.
CW082
EUDAMED did not publish a description for this code.
CW085
EUDAMED did not publish a description for this code.
CW162
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW175
EUDAMED did not publish a description for this code.
CW178
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: Digest-EUR
UDI-DI code: 03366160500260
Basic UDI-DI: 3661605DD0DIG00B6
Reference / catalog number: DD0DIG00-AI
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: 6
Additional product description: The Digest-EUR is a reagent for the fluidification of mucous biological samples.
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.

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