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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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Perometer — 4 UDI-DI variants, MDR (Pero-System GmbH)

MD Atlas
Pero-System GmbH

Data from EUDAMED, last updated May 23, 2026

Perometer

426242765PerometerRH

4 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: Pero-System GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426242765PerometerRH
Device name: Perometer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: Pero-System GmbH
SRN: DE-MF-000013314
Country: Germany
Email: info@pero-system.de
Phone: +49 202 31713 222

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01J1DERT5ZVHPT2TJCJECTDV3D

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

Perometer 350 MT04262427650015
Perometer 1000 MT04262427650039
Perometer 1400 MT04262427650046
Perometer 400 MT04262427650022