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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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Patient transfer device for operating… — 2 UDI-DI variants, MDR

MD Atlas
RAMED Kopřivnice s.r.o.

Data from EUDAMED, last updated May 23, 2026

Patient transfer device for operating rooms PPZ 01

859420869PPZ01RE

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: RAMED Kopřivnice s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859420869PPZ01RE
Device name: Patient transfer device for operating rooms PPZ 01
Device model: PPZ
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 17, 2026

Manufacturer & authorised representative

Manufacturer

Name: RAMED Kopřivnice s.r.o.
SRN: CZ-MF-000043587
Country: Czechia
Email: raska@ramed.cz
Phone: +420 602 731 912, +420 556 802 321

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KPDNBHDJWZWQGJCEVF62Z809

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

PPZ01-0108594208690795
PPZ01-0008594208690184