eudamed_udi
Primary ID: 04260586040760
Deckel für Mehrweg-Sekretbehälter Allegra M30 (UDI 04260586040760)
Manufactured by ASSKEA GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Deckel für Mehrweg-Sekretbehälter Allegra M30 - Primary ID 04260586040760
Device Regulatory Overview
The Deckel für Mehrweg-Sekretbehälter Allegra M30 (Model/Catalog Number: 1510214HL5) 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
- 1510214HL5
- Product Code / EMDN
- A060399
- Device Name
- Mehrwegbehälter
- Database Sync Date
- 2026-08-09 18:25:30
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 Deckel für Mehrweg-Sekretbehälter Allegra M30?
The registered manufacturer of record for Deckel für Mehrweg-Sekretbehälter Allegra M30 is ASSKEA GmbH.
What is the Primary UDI-DI identifier for Deckel für Mehrweg-Sekretbehälter Allegra M30?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260586040760.
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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