Ambulatory insulin infusion pump software, patient-dosing - UK MHRA Medical Device Registration

Ambulatory insulin infusion pump software, patient-dosing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204819. The device is manufactured by mySugr GmbH from Austria, classified as General Medical Device. The authorized representative in the UK is Roche Diagnostics Limited.

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Ambulatory insulin infusion pump software, patient-dosing

MHRA Device ID: 204819•Ref: 204819

Device Type

General Medical Device

Devices

Ambulatory insulin infusion pump software, patient-dosing

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Nov 9, 2024

Manufacturer Information

Name

mySugr GmbH

Address

Trattnerhof 1/5 OG

Vienna, Austria

Created Date

Nov 7, 2024

Authorized Representative

Name

Roche Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Roche Diagnostics Limited Charles Avenue

Burgess Hill, West Sussex, United Kingdom

Postcode: RH15 9RY

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Ambulatory insulin infusion pump software, patient-dosing - UK MHRA Medical Device Registration

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