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Primary ID: 05999526660391
Promtmarket IK (UDI 05999526660391)
Manufactured by PROMT MARKET KFT.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Promtmarket IK - Primary ID 05999526660391
Device Regulatory Overview
The Promtmarket IK (Model/Catalog Number: IK1,5) is a medical device manufactured by PROMT MARKET KFT.. This product is indexed under FDA Product Code / Category Classification T030599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IK1,5
- Product Code / EMDN
- T030599
- Device Name
- irrigátor kanna
- Database Sync Date
- 2026-08-09 18:28:12
Full Regulatory Attributes
đź”’ Token Gated
{
"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 Promtmarket IK?
The registered manufacturer of record for Promtmarket IK is PROMT MARKET KFT..
What is the Primary UDI-DI identifier for Promtmarket IK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05999526660391.
What classification code is assigned to this device?
This device is registered under product classification code T030599.
Similar Classification Devices (T030599)
Other Devices by PROMT MARKET KFT.
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