eudamed_udi
Primary ID: 04260586042269
visioBag (UDI 04260586042269)
Manufactured by ASSKEA GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for visioBag - Primary ID 04260586042269
Device Regulatory Overview
The visioBag (Model/Catalog Number: 100281) is a medical device manufactured by ASSKEA GmbH. This product is indexed under FDA Product Code / Category Classification A060399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100281
- Product Code / EMDN
- A060399
- Device Name
- Mehrwegbehälter
- Database Sync Date
- 2026-08-09 17:21:56
Full Regulatory Attributes
đź”’ Token Gated
{
"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 visioBag?
The registered manufacturer of record for visioBag is ASSKEA GmbH.
What is the Primary UDI-DI identifier for visioBag?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260586042269.
What classification code is assigned to this device?
This device is registered under product classification code A060399.
Similar Classification Devices (A060399)
Other Devices by ASSKEA GmbH
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