eudamed_udi
Primary ID: 08594224180140
Unspecified Brand (UDI 08594224180140)
Manufactured by Medirekt partner s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08594224180140
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 574301) is a medical device manufactured by Medirekt partner s.r.o.. This product is indexed under FDA Product Code / Category Classification G020301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 574301
- Product Code / EMDN
- G020301
- Device Name
- Rectal tube
- Database Sync Date
- 2026-08-09 16:59:05
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Medirekt partner s.r.o..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594224180140.
What classification code is assigned to this device?
This device is registered under product classification code G020301.
Similar Classification Devices (G020301)
Other Devices by Medirekt partner s.r.o.
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