Respimat (UDI 04065477001024)
Manufactured by Boehringer Ingelheim Pharma GmbH & Co. KG
Device Regulatory Overview
The Respimat (Model/Catalog Number: INH RES A5.3.1 SPI 60HUB GUMD / 84970) is a medical device manufactured by Boehringer Ingelheim Pharma GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification R03010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INH RES A5.3.1 SPI 60HUB GUMD / 84970
- Product Code / EMDN
- R03010302
- Device Name
- Respimat
- Database Sync Date
- 2026-08-09 17:15:21
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Respimat?
The registered manufacturer of record for Respimat is Boehringer Ingelheim Pharma GmbH & Co. KG.
What is the Primary UDI-DI identifier for Respimat?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04065477001024.
What classification code is assigned to this device?
This device is registered under product classification code R03010302.
Similar Classification Devices (R03010302)
Other Devices by Boehringer Ingelheim Pharma GmbH & Co. KG
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