eudamed_udi
Primary ID: 04032651091607
mikrozid AF liquid (UDI 04032651091607)
Manufactured by Schülke & Mayr GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for mikrozid AF liquid - Primary ID 04032651091607
Device Regulatory Overview
The mikrozid AF liquid (Model/Catalog Number: 109160) is a medical device manufactured by Schülke & Mayr GmbH. This product is indexed under FDA Product Code / Category Classification D0799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 109160
- Product Code / EMDN
- D0799
- Device Name
- Mikrozid AF
- Database Sync Date
- 2026-08-09 16:28:44
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 mikrozid AF liquid?
The registered manufacturer of record for mikrozid AF liquid is Schülke & Mayr GmbH.
What is the Primary UDI-DI identifier for mikrozid AF liquid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04032651091607.
What classification code is assigned to this device?
This device is registered under product classification code D0799.
Similar Classification Devices (D0799)
Other Devices by Schülke & Mayr GmbH
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