eudamed_udi
Primary ID: 04537693005099
ViE (UDI 04537693005099)
Manufactured by Asahi Kasei Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ViE - Primary ID 04537693005099
Device Regulatory Overview
The ViE (Model/Catalog Number: ViE-21A) is a medical device manufactured by Asahi Kasei Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification F01060303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ViE-21A
- Product Code / EMDN
- F01060303
- Device Name
- ASAHI ViE-A SERIES DIALYZER
- Database Sync Date
- 2026-08-09 16:44:52
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 ViE?
The registered manufacturer of record for ViE is Asahi Kasei Medical Co., Ltd..
What is the Primary UDI-DI identifier for ViE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04537693005099.
What classification code is assigned to this device?
This device is registered under product classification code F01060303.
Similar Classification Devices (F01060303)
Other Devices by Asahi Kasei Medical Co., Ltd.
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