gudid
Primary ID: Biobeam 2000
dose-map (UDI Biobeam 2000)
Manufactured by ASHLAND SPECIALTY INGREDIENTS G.P.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for dose-map - Primary ID Biobeam 2000
Device Regulatory Overview
The dose-map (Model/Catalog Number: Biobeam 2000) is a medical device manufactured by ASHLAND SPECIALTY INGREDIENTS G.P.. This product is indexed under FDA Product Code / Category Classification IXA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Biobeam 2000
- Product Code / EMDN
- IXA
- Device Name
- blood irradiator dosimetry system
- Database Sync Date
- 2026-08-09 09:09:51
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 dose-map?
The registered manufacturer of record for dose-map is ASHLAND SPECIALTY INGREDIENTS G.P..
What is the Primary UDI-DI identifier for dose-map?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Biobeam 2000.
What classification code is assigned to this device?
This device is registered under product classification code IXA.
Similar Classification Devices (IXA)
Other Devices by ASHLAND SPECIALTY INGREDIENTS G.P.
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