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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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Pacmed Critical — 9 UDI-DI variants, MDR (Pacmed B.V.)

MD Atlas
Pacmed B.V.

Data from EUDAMED, last updated May 30, 2026

Pacmed Critical

872090823PCX8

9 UDI-DI variants

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

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

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 872090823PCX8
Device name: Pacmed Critical
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: Pacmed B.V.
SRN: NL-MF-000010920
Country: Netherlands
Email: info@pacmed.nl

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01HFY1T4DQTHAF576Y8TEB6S7X

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

Pacmed Critical08720908230126
V3.2.008720908230058
V4.0.008720908230119
Pacmed Critical08720908230041
V3.3.008720908230065
V3.7.008720908230102
V3.4.008720908230072
V3.5.008720908230089
V3.6.008720908230096