eudamed_udi
Primary ID: 04260586040005
ASSKEA M20 (UDI 04260586040005)
Manufactured by ASSKEA GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ASSKEA M20 - Primary ID 04260586040005
Device Regulatory Overview
The ASSKEA M20 (Model/Catalog Number: 100003-3) 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
- 100003-3
- Product Code / EMDN
- Z12159009
- Device Name
- Secretion Aspirators
- Database Sync Date
- 2026-08-09 17:16:12
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 ASSKEA M20?
The registered manufacturer of record for ASSKEA M20 is ASSKEA GmbH.
What is the Primary UDI-DI identifier for ASSKEA M20?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260586040005.
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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