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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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Aneroid Blood Pressure Kit — 2 UDI-DI variants, MDR (B.Well Swiss AG)

MD Atlas
B.Well Swiss AG

Data from EUDAMED, last updated May 23, 2026

Aneroid Blood Pressure Kit

764015639MDN1207_1U7

2 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: B.Well Swiss AG

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 764015639MDN1207_1U7
Device name: Aneroid Blood Pressure Kit
Device model: MED-61, MED-62, MED-63, PRO-60
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: B.Well Swiss AG
SRN: CH-MF-000012588
Country: Switzerland
Email: info@bwell-swiss.ch

Authorised representative

Name: Blue Broccoli GmbH
SRN: LI-AR-000000233
Country: Liechtenstein

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JRWBCHR40R0FJD7HY2VTQW92

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

MED-62 Aneroid Blood Pressure Kit07640156395938
MED-63 Aneroid Blood Pressure Kit07640156395945