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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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Compressor nebulizer — 4 UDI-DI variants, MDR (B.Well Swiss AG)

MD Atlas
B.Well Swiss AG

Data from EUDAMED, last updated May 23, 2026

Compressor nebulizer

764015639MDA0307_1M8

4 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: B.Well Swiss AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 764015639MDA0307_1M8
Device name: Compressor nebulizer
Device model: MED-120, PRO-110, PRO-115, TH-130, MED-111, MED-130
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JRA98HVJXCX8N7C77TCXFX9E

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-120 Compressor nebulizer07640156396195
MED-130 Compressor nebulizer07640156398472
PRO-110 Medical nebulizer07640156393101
PRO-115 Medical nebulizer07640156393118