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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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Citra-Lock™ Catheter lock solution — 3 UDI-DI variants, MDR

MD Atlas
Dirinco B.V.

Data from EUDAMED, last updated May 31, 2026

Citra-Lock™ Catheter lock solution

8717931430123456789RS

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Dirinco B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8717931430123456789RS
Device name: Citra-Lock™ Catheter lock solution
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Dirinco B.V.
SRN: NL-MF-000002150
Country: Netherlands
Email: info@dirinco.com
Phone: 0031881501100

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KQA1H3B4ZJY289SS3WF5V5NK

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

2406020308717931430340
2406020108717931430371
2406020208717931430319