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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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ZIEHL-NEELSEN FUCSINA FENICATA — 2 UDI-DI variants, IVDR

MD Atlas
Titolchimica S.p.A.

Data from EUDAMED, last updated May 30, 2026

ZIEHL-NEELSEN FUCSINA FENICATA

805005413TC78800TM

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Titolchimica S.p.A.

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 805005413TC78800TM
Device name: ZIEHL-NEELSEN FUCSINA FENICATA
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Titolchimica S.p.A.
SRN: IT-MF-000028986
Country: Italy
Email: info@titolchimica.it
Phone: +390425492644

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRGMBY9GCCBD7YDFV7B2GVKC

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

TC78800PP08050054130958
TC78800QQ08050054130965