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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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EASY PULSE — 2 UDI-DI variants, MDR (SCHILLER AG)

MD Atlas
SCHILLER AG

Data from EUDAMED, last updated May 23, 2026

EASY PULSE

76133650000000024W

2 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: SCHILLER AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 76133650000000024W
Device name: EASY PULSE
Device model: EASY PULSE Base Device IP43 Version (modified)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: SCHILLER AG
SRN: CH-MF-000012722
Country: Switzerland
Email: info@schiller.ch
Phone: +41 41 766 42 42

Authorised representative

Name: SCHILLER Medizintechnik GmbH
SRN: DE-AR-000006934
Country: Germany
Phone: +49 89 629981 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GA27QRFXV1STEQEHAT8V7P9J

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

EASY PULSE Base device IP33 version07613365001679
EASY PULSE Base device IP43 version (modified)07613365001853