T-kulcs (UDI 05996527007682)
Manufactured by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.
Device Regulatory Overview
The T-kulcs (Model/Catalog Number: 222900005) 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
- 222900005
- Product Code / EMDN
- L0999
- Device Name
- Wrench
- Database Sync Date
- 2026-08-09 16:29:30
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of T-kulcs?
The registered manufacturer of record for T-kulcs is Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft..
What is the Primary UDI-DI identifier for T-kulcs?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05996527007682.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint