eudamed_udi
Primary ID: 08052747954407
Volumed Heidelberger Extension Line (UDI 08052747954407)
Manufactured by PHOENIX S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Volumed Heidelberger Extension Line - Primary ID 08052747954407
Device Regulatory Overview
The Volumed Heidelberger Extension Line (Model/Catalog Number: 4001501001) is a medical device manufactured by PHOENIX S.R.L.. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4001501001
- Product Code / EMDN
- A03020101
- Device Name
- Dispositivi per Infusione ed Aspirazione
- Database Sync Date
- 2026-08-09 16:28:45
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 Volumed Heidelberger Extension Line?
The registered manufacturer of record for Volumed Heidelberger Extension Line is PHOENIX S.R.L..
What is the Primary UDI-DI identifier for Volumed Heidelberger Extension Line?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052747954407.
What classification code is assigned to this device?
This device is registered under product classification code A03020101.
Similar Classification Devices (A03020101)
Other Devices by PHOENIX S.R.L.
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