Ruchoma kładka, podwieszany mostek (UDI 05907097261022)
Manufactured by Si-iS Paweł Wyszyński
Device Regulatory Overview
The Ruchoma kładka, podwieszany mostek (Model/Catalog Number: 5907097261022) is a medical device manufactured by Si-iS Paweł Wyszyński. This product is indexed under FDA Product Code / Category Classification Y0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5907097261022
- Product Code / EMDN
- Y0599
- Device Name
- Ruchoma kładka, podwieszany mostek
- Database Sync Date
- 2026-08-09 16:46:41
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 Ruchoma kładka, podwieszany mostek?
The registered manufacturer of record for Ruchoma kładka, podwieszany mostek is Si-iS Paweł Wyszyński.
What is the Primary UDI-DI identifier for Ruchoma kładka, podwieszany mostek?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907097261022.
What classification code is assigned to this device?
This device is registered under product classification code Y0599.
Similar Classification Devices (Y0599)
Other Devices by Si-iS Paweł Wyszyński
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