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

BIDON 10L FORMALDEHYDE 4% pH7 — IVDR Class A IVDR by LAURYPATH

MD Atlas
LAURYPATH

EUDAMED last updated this device on Sep 26, 2022

BIDON 10L FORMALDEHYDE 4% pH7

37015164FORMOL4KJ

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: LAURYPATH
UDI-DI code: 03701516400588
Reference / catalog number: 40877-41-LAB

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

Related devices

10% Neutral Buffered Formalin 1 L (x12)37015164FORMOL4KJOn the market 10% Neutral Buffered Formalin 10 L (x1)37015164FORMOL4KJOn the market 10% Neutral Buffered Formalin 1000/500 ML (x1)37015164FORMOL4KJOn the market 10% NEUTRAL BUFFERED FORMALIN 10L37015164FORMOL4KJOn the market 10% Neutral Buffered Formalin 125/60 ML - YELLOW CAPS (x24)37015164FORMOL4KJOn the market

Critical warnings

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

CW083
EUDAMED did not publish a description for this code.
CW093
EUDAMED did not publish a description for this code.
CW094
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: BIDON 10L FORMALDEHYDE 4% pH7
UDI-DI code: 03701516400588
Basic UDI-DI: 37015164FORMOL4KJ
Reference / catalog number: 40877-41-LAB
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)

W01030705FIXING REAGENTS (HISTOLOGY/CYTOLOGY)

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.