Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

10% NEUTRAL BUFFERED FORMALIN 5 LT — IVDR Class A IVDR

MD Atlas
Diapath S.p.A. società a socio unico

EUDAMED last updated this device on Apr 27, 2026

10% NEUTRAL BUFFERED FORMALIN 5 LT

8033895W01030705For10%RZ

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Diapath S.p.A. società a socio unico
UDI-DI code: 08033895005401
Reference / catalog number: F0046

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?

View device family (Basic UDI)

Manufacturer information

Organization name: Diapath S.p.A. società a socio unico
SRN: IT-MF-000027016
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW999
Consult Material Safety data sheet

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: 10% NEUTRAL BUFFERED FORMALIN 5 LT
UDI-DI code: 08033895005401
Basic UDI-DI: 8033895W01030705For10%RZ
Reference / catalog number: F0046
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: PRIMARY FIXATIVE CONTAINING 4% FORMALDEHYDE READY-TO-USE, PH BETWEEN 7.2 AND 7.4
Additional information URL: https://www.diapath.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W01030705FIXING REAGENTS (HISTOLOGY/CYTOLOGY)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Become a partner of MD Atlas

Related devices

XYLENE 1 LT8033895W01030799XyleneT3On the market 10% NEUTRAL BUFFERED FORMALIN 1 LT8033895W01030705For10%RZOn the market 10% NEUTRAL BUFFERED FORMALIN 10 LT8033895W01030705For10%RZOn the market 10% NEUTRAL BUFFERED FORMALIN 2.5 LT8033895W01030705For10%RZOn the market 10% NEUTRAL BUFFERED FORMALIN 20 LT8033895W01030705For10%RZOn 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.