STABILIZZATORE DI ROTULA E LCL-LCM E FORO TAGLIA XXXL (UDI 08028718820552)
Manufactured by PAVIS SPA
Device Regulatory Overview
The STABILIZZATORE DI ROTULA E LCL-LCM E FORO TAGLIA XXXL (Model/Catalog Number: 042BL XXXL) is a medical device manufactured by PAVIS SPA. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 042BL XXXL
- Product Code / EMDN
- Y061209
- Device Name
- LINEA GAMBA GINOCCHIO
- Database Sync Date
- 2026-08-09 16:30:43
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 STABILIZZATORE DI ROTULA E LCL-LCM E FORO TAGLIA XXXL?
The registered manufacturer of record for STABILIZZATORE DI ROTULA E LCL-LCM E FORO TAGLIA XXXL is PAVIS SPA.
What is the Primary UDI-DI identifier for STABILIZZATORE DI ROTULA E LCL-LCM E FORO TAGLIA XXXL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718820552.
What classification code is assigned to this device?
This device is registered under product classification code Y061209.
Similar Classification Devices (Y061209)
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