eudamed_udi
Primary ID: ++G086808021
Anmischblock, mittel (UDI ++G086808021)
Manufactured by M. G. Kurth GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anmischblock, mittel - Primary ID ++G086808021
Device Regulatory Overview
The Anmischblock, mittel (Model/Catalog Number: 80802) is a medical device manufactured by M. G. Kurth GmbH. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80802
- Product Code / EMDN
- Q010503
- Device Name
- Anmischblock
- Database Sync Date
- 2026-08-09 16:29:10
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 Anmischblock, mittel?
The registered manufacturer of record for Anmischblock, mittel is M. G. Kurth GmbH.
What is the Primary UDI-DI identifier for Anmischblock, mittel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ++G086808021.
What classification code is assigned to this device?
This device is registered under product classification code Q010503.
Similar Classification Devices (Q010503)
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