eudamed_udi
Primary ID: 42607100508496
Hexadermal MD Spray (UDI 42607100508496)
Manufactured by BABGENCEL GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hexadermal MD Spray - Primary ID 42607100508496
Device Regulatory Overview
The Hexadermal MD Spray (Model/Catalog Number: 20HX01-LE0011000) is a medical device manufactured by BABGENCEL GmbH. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20HX01-LE0011000
- Product Code / EMDN
- D0701
- Device Name
- Alcohol Based Disinfection Spray
- Database Sync Date
- 2026-08-09 16:48:41
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 Hexadermal MD Spray?
The registered manufacturer of record for Hexadermal MD Spray is BABGENCEL GmbH.
What is the Primary UDI-DI identifier for Hexadermal MD Spray?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42607100508496.
What classification code is assigned to this device?
This device is registered under product classification code D0701.
Similar Classification Devices (D0701)
Other Devices by BABGENCEL GmbH
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