eudamed_udi
Primary ID: 04260044630069
Zantomed Mischpistole 4:1/10:1 (UDI 04260044630069)
Manufactured by Zantomed GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zantomed Mischpistole 4:1/10:1 - Primary ID 04260044630069
Device Regulatory Overview
The Zantomed Mischpistole 4:1/10:1 (Model/Catalog Number: DIGUNNT10) is a medical device manufactured by Zantomed GmbH. This product is indexed under FDA Product Code / Category Classification Q0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DIGUNNT10
- Product Code / EMDN
- Q0199
- Device Name
- Mischpistole für Kartuschensysteme
- Database Sync Date
- 2026-08-09 17:16:35
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 Zantomed Mischpistole 4:1/10:1?
The registered manufacturer of record for Zantomed Mischpistole 4:1/10:1 is Zantomed GmbH.
What is the Primary UDI-DI identifier for Zantomed Mischpistole 4:1/10:1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260044630069.
What classification code is assigned to this device?
This device is registered under product classification code Q0199.
Similar Classification Devices (Q0199)
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