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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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myPump+ Reservoir — 1 UDI-DI variant, MDR (mylife Diabetes Care AG)

MD Atlas
mylife Diabetes Care AG

Data from EUDAMED, last updated Jun 2, 2026

myPump+ Reservoir

764028148000122

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: mylife Diabetes Care AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764028148000122
Device name: myPump+ Reservoir
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: mylife Diabetes Care AG
SRN: CH-MF-000044659
Country: Switzerland
Email: regulatory-affairs@mylife-diabetescare.com
Phone: +41 58 234 71 84

Authorised representative

Name: mylife Distribution GmbH
SRN: DE-AR-000005922
Country: Germany

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSX6TC7MBK5ZRABYSEDBVT8G

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

myPump+ Reservoir07640281480059