Kalapács (UDI 05996527002489)
Manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
Device Regulatory Overview
The Kalapács (Model/Catalog Number: 210030000) is a medical device manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.. This product is indexed under FDA Product Code / Category Classification L0903 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 210030000
- Product Code / EMDN
- L0903
- Device Name
- Hammer
- Database Sync Date
- 2026-08-09 16:30:18
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 Kalapács?
The registered manufacturer of record for Kalapács is Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft..
What is the Primary UDI-DI identifier for Kalapács?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05996527002489.
What classification code is assigned to this device?
This device is registered under product classification code L0903.
Similar Classification Devices (L0903)
Other Devices by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
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