Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

INH RES A5.2 BERO 120HUB GUMD /… — Class IIb MDR

MD Atlas
Boehringer Ingelheim Pharma GmbH & Co. KG

EUDAMED last updated this device on Dec 9, 2024

INH RES A5.2 BERO 120HUB GUMD / 84976

4065477RESPIMATEJ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Boehringer Ingelheim Pharma GmbH & Co. KG
UDI-DI code: 04065477001017
Reference / catalog number: INH RES A5.2 BERO 120HUB GUMD / 84976

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: Boehringer Ingelheim Pharma GmbH & Co. KG
SRN: DE-MF-000015595
Manufacturer status: Active

Related devices

HH OEFFHI KAMMER AUS PC EU/ROW / 877124065477HANDIHALERRHOn the market INH RES A5.9.1 R Olodaterol / 870294065477RESPIMATEJOn the market INH RES A5.3.1 R SPIRIVA / 870284065477RESPIMATEJOn the market INH RES A5.10.1 R T+O / 870304065477RESPIMATEJOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2004	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04065477001017
Basic UDI-DI: 4065477RESPIMATEJ
Reference / catalog number: INH RES A5.2 BERO 120HUB GUMD / 84976
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

R03010302AEROSOL PORTABLE INHALERS

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification