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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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Aktiia Bracelet G1 - Blood Pressure… — 2 UDI-DI variants, MDR

MD Atlas
Aktiia SA

Data from EUDAMED, last updated May 23, 2026

Aktiia Bracelet G1 - Blood Pressure Monitor

7649998849AKBraceletYW

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Aktiia SA

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 7649998849AKBraceletYW
Device name: Aktiia Bracelet G1 - Blood Pressure Monitor
Device model: G1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 6, 2024

Manufacturer & authorised representative

Manufacturer

Name: Aktiia SA
SRN: CH-MF-000015833
Country: Switzerland
Email: eudamed@aktiia.com

Authorised representative

Name: Veranex Germany GmbH
SRN: DE-AR-000005578
Country: Germany

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01HX7Q5HKXZR7CZMZDAA2QYX8V

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

Hilo Band17649998849088
Hilo Band (Aktiia Bracelet G1)17649998849019