eudamed_udi
Primary ID: 04260586042290
ASSKEA proVisio M28 (UDI 04260586042290)
Manufactured by ASSKEA GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASSKEA proVisio M28 - Primary ID 04260586042290
Device Regulatory Overview
The ASSKEA proVisio M28 (Model/Catalog Number: 100739RE-2) is a medical device manufactured by ASSKEA GmbH. This product is indexed under FDA Product Code / Category Classification Z12159009 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100739RE-2
- Product Code / EMDN
- Z12159009
- Device Name
- Secretion Aspirators
- Database Sync Date
- 2026-08-09 16:49:44
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 ASSKEA proVisio M28?
The registered manufacturer of record for ASSKEA proVisio M28 is ASSKEA GmbH.
What is the Primary UDI-DI identifier for ASSKEA proVisio M28?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260586042290.
What classification code is assigned to this device?
This device is registered under product classification code Z12159009.
Similar Classification Devices (Z12159009)
Other Devices by ASSKEA GmbH
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