eudamed_udi
Primary ID: 07612449145308
Meliseptol® (UDI 07612449145308)
Manufactured by B. Braun Medical AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Meliseptol® - Primary ID 07612449145308
Device Regulatory Overview
The Meliseptol® (Model/Catalog Number: 19804) is a medical device manufactured by B. Braun Medical AG. This product is indexed under FDA Product Code / Category Classification D0799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19804
- Product Code / EMDN
- D0799
- Device Name
- Meliseptol Foam pure
- Database Sync Date
- 2026-08-09 16:48:13
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 Meliseptol®?
The registered manufacturer of record for Meliseptol® is B. Braun Medical AG.
What is the Primary UDI-DI identifier for Meliseptol®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07612449145308.
What classification code is assigned to this device?
This device is registered under product classification code D0799.
Similar Classification Devices (D0799)
Other Devices by B. Braun Medical AG
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