Ínleválasztó (UDI 05996527000782)
Manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
Device Regulatory Overview
The Ínleválasztó (Model/Catalog Number: 188370000) is a medical device manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.. This product is indexed under FDA Product Code / Category Classification L0999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 188370000
- Product Code / EMDN
- L0999
- Device Name
- Guiding Devices
- Database Sync Date
- 2026-08-09 16:45:08
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 Ínleválasztó?
The registered manufacturer of record for Ínleválasztó is Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft..
What is the Primary UDI-DI identifier for Ínleválasztó?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05996527000782.
What classification code is assigned to this device?
This device is registered under product classification code L0999.
Similar Classification Devices (L0999)
Other Devices by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
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