GM-K8 L (UDI 05999542979941)
Manufactured by PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
Device Regulatory Overview
The GM-K8 L (Model/Catalog Number: GM-K8 L) is a medical device manufactured by PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GM-K8 L
- Product Code / EMDN
- Y061209
- Device Name
- TÉRDORTÉZISEK
- Database Sync Date
- 2026-08-09 16:30:08
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 GM-K8 L?
The registered manufacturer of record for GM-K8 L is PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság.
What is the Primary UDI-DI identifier for GM-K8 L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05999542979941.
What classification code is assigned to this device?
This device is registered under product classification code Y061209.
Similar Classification Devices (Y061209)
Other Devices by PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
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