gudid
Primary ID: MP01745
HME HumidStar 2 (UDI MP01745)
Manufactured by Drgerwerk AG & Co. KGaA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HME HumidStar 2 - Primary ID MP01745
Device Regulatory Overview
The HME HumidStar 2 (Model/Catalog Number: MP01745) is a medical device manufactured by Drgerwerk AG & Co. KGaA. This product is indexed under FDA Product Code / Category Classification BYD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MP01745
- Product Code / EMDN
- BYD
- Device Name
- Database Sync Date
- 2026-08-09 09:11:31
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 HME HumidStar 2?
The registered manufacturer of record for HME HumidStar 2 is Drgerwerk AG & Co. KGaA.
What is the Primary UDI-DI identifier for HME HumidStar 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MP01745.
What classification code is assigned to this device?
This device is registered under product classification code BYD.
Similar Classification Devices (BYD)
Other Devices by Drgerwerk AG & Co. KGaA
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