Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

01256_33 — IVDR Class A IVDR by LABORATOIRE VERBIESE

MD Atlas
LABORATOIRE VERBIESE

EUDAMED last updated this device on May 14, 2026

01256_33

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: 03701399901813
Reference / catalog number: 01256_33

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

Fixateur de Duboscq-Brasil dans 60 ml - 20 ml37013999512936CON607UOn the market Formol tamponné pbs 4 % - 10 ml / 20 ml37013999512029CON202TOn the market Formol tamponné pbs 4 % - 10 ml / 40 ml37013999512029CON402ZOn the market Formol tamponné pbs 4 % - 100 ml / 180 ml37013999512029CON180F2On the market Formol tamponné pbs 4 % - 120 ml / 180 ml37013999512029CON180F2On 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.

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: 03701399901813
Basic UDI-DI: 3701399927256SOLTA
Reference / catalog number: 01256_33
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