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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

Xylene — IVDR Class A IVDR by LAURYPATH

MD Atlas
LAURYPATH

EUDAMED last updated this device on Oct 14, 2025

Xylene

37015164XYLENEQ6

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: LAURYPATH
UDI-DI code: 03701516402100
Reference / catalog number: 6615-LP

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Manufacturer information

Organization name: LAURYPATH
SRN: FR-MF-000020948
Manufacturer status: Active

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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.

Critical warnings

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

CW077
EUDAMED did not publish a description for this code.
CW080
EUDAMED did not publish a description for this code.
CW082
EUDAMED did not publish a description for this code.
CW088
EUDAMED did not publish a description for this code.
CW102
EUDAMED did not publish a description for this code.
CW104
EUDAMED did not publish a description for this code.
CW058
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Netherlands; available across 1 country total.

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

Device identification

Trade name: Xylene
UDI-DI code: 03701516402100
Basic UDI-DI: 37015164XYLENEQ6
Reference / catalog number: 6615-LP
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: 4
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)

W01030799HISTOLOGY / CYTOLOGY REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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Expiration date
Manufacturing date
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Software identification