Peremes vápabenyomó fej (UDI 05996527013232)
Manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
Device Regulatory Overview
The Peremes vápabenyomó fej (Model/Catalog Number: 419300006) is a medical device manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 419300006
- Product Code / EMDN
- L091001
- Device Name
- Impactor and Extraktor
- Database Sync Date
- 2026-08-09 16:28:57
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 Peremes vápabenyomó fej?
The registered manufacturer of record for Peremes vápabenyomó fej is Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft..
What is the Primary UDI-DI identifier for Peremes vápabenyomó fej?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05996527013232.
What classification code is assigned to this device?
This device is registered under product classification code L091001.
Similar Classification Devices (L091001)
Other Devices by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
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