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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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Natriumcitrat Lösung 3,13% 10x1ml — 11 UDI-DI variants, IVDR

MD Atlas
Eifelfango Chem. Pharm. Werk GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Natriumcitrat Lösung 3,13% 10x1ml

PP07140NATRI07

11 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: Eifelfango Chem. Pharm. Werk GmbH & Co. KG

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: PP07140NATRI07
Device name: Natriumcitrat Lösung 3,13% 10x1ml
Issuing agency: IFA
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Eifelfango Chem. Pharm. Werk GmbH & Co. KG
SRN: DE-MF-000009424
Country: Germany
Email: email@eifelfango.de
Phone: 0264136061

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01KG50M8M7WH235ZFCHDQFWQPX

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

IFA110070269931
IFA110257259747
IFAPP7140NATRI07
IFA110076215874
IFA110070271388
IFA110257260541
IFA110070275900
IFA110136184678
IFA110076216440
IFA110070270725
IFA110070274210