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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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Respimat — 4 UDI-DI variants, MDR

MD Atlas
Boehringer Ingelheim Pharma GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

Respimat

4065477RESPIMATEJ

4 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Boehringer Ingelheim Pharma GmbH & Co. KG

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 4065477RESPIMATEJ
Device name: Respimat
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Boehringer Ingelheim Pharma GmbH & Co. KG
SRN: DE-MF-000015595
Country: Germany
Email: info@boehringer-ingelheim.de
Phone: +49 800 77 90900

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JE66GCSD029J4V6XMT75JQ5P

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

INH RES A5.3.1 R SPIRIVA / 8702804065477001062
INH RES A5.2 BERO 120HUB GUMD / 8497604065477001017
INH RES A5.10.1 R T+O / 8703004065477001086
INH RES A5.9.1 R Olodaterol / 8702904065477001079