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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

01256_35 — IVDR Class A IVDR by LABORATOIRE VERBIESE

MD Atlas
LABORATOIRE VERBIESE

EUDAMED last updated this device on May 14, 2026

01256_35

3701399927256SOLTA

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: LABORATOIRE VERBIESE
UDI-DI code: 03701399901790
Reference / catalog number: 01256_35

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Manufacturer information

Organization name: LABORATOIRE VERBIESE
SRN: FR-MF-000023445
Manufacturer status: Active

Critical warnings

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

CW057
EUDAMED did not publish a description for this code.
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.
CW091
EUDAMED did not publish a description for this code.
CW102
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03701399901790
Basic UDI-DI: 3701399927256SOLTA
Reference / catalog number: 01256_35
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: —
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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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.