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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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PacePress - CIED implant site… — 2 UDI-DI variants, MDR

MD Atlas
Medinice S.A.

Data from EUDAMED, last updated May 31, 2026

PacePress - CIED implant site compression device, standard size

59038873766PP018G

2 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: Medinice S.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59038873766PP018G
Device name: PacePress - CIED implant site compression device, standard size
Device model: PP01-01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medinice S.A.
SRN: PL-MF-000026941
Country: Poland
Email: biuro@medinice.pl
Phone: +48 725 500 051

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQCJGP0M050EMPDPVQZJF7EM

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

PP01-11 05903887376693
PP01-01 05903887376631