eudamed_udi
Primary ID: 05998177100027
BÉABA MINIDOO (UDI 05998177100027)
Manufactured by Rokána Kft.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BÉABA MINIDOO - Primary ID 05998177100027
Device Regulatory Overview
The BÉABA MINIDOO (Model/Catalog Number: 002) is a medical device manufactured by Rokána Kft.. This product is indexed under FDA Product Code / Category Classification Z12159009 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002
- Product Code / EMDN
- Z12159009
- Device Name
- Szájjal szívható orrszívó
- Database Sync Date
- 2026-08-09 16:51:06
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 BÉABA MINIDOO?
The registered manufacturer of record for BÉABA MINIDOO is Rokána Kft..
What is the Primary UDI-DI identifier for BÉABA MINIDOO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05998177100027.
What classification code is assigned to this device?
This device is registered under product classification code Z12159009.
Similar Classification Devices (Z12159009)
Other Devices by Rokána Kft.
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