eudamed_udi
Primary ID: 04251816802494
BES-1062/INF (UDI 04251816802494)
Manufactured by AGA Sanitätsartikel GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BES-1062/INF - Primary ID 04251816802494
Device Regulatory Overview
The BES-1062/INF (Model/Catalog Number: 100) is a medical device manufactured by AGA Sanitätsartikel GmbH. This product is indexed under FDA Product Code / Category Classification V080299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100
- Product Code / EMDN
- V080299
- Device Name
- Blutentnahmestuhl
- Database Sync Date
- 2026-08-09 16:49:25
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 BES-1062/INF?
The registered manufacturer of record for BES-1062/INF is AGA Sanitätsartikel GmbH.
What is the Primary UDI-DI identifier for BES-1062/INF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251816802494.
What classification code is assigned to this device?
This device is registered under product classification code V080299.
Similar Classification Devices (V080299)
Other Devices by AGA Sanitätsartikel GmbH
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