eudamed_udi
Primary ID: 08028718350554
STABILIZZATORE DI ROTULA E LCL-LCM TAGLIA XXXL (UDI 08028718350554)
Manufactured by PAVIS SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STABILIZZATORE DI ROTULA E LCL-LCM TAGLIA XXXL - Primary ID 08028718350554
Device Regulatory Overview
The STABILIZZATORE DI ROTULA E LCL-LCM TAGLIA XXXL (Model/Catalog Number: 041BL 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
- 041BL XXXL
- Product Code / EMDN
- Y061209
- Device Name
- LINEA GAMBA GINOCCHIO
- Database Sync Date
- 2026-08-09 16:51:04
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 TAGLIA XXXL?
The registered manufacturer of record for STABILIZZATORE DI ROTULA E LCL-LCM TAGLIA XXXL is PAVIS SPA.
What is the Primary UDI-DI identifier for STABILIZZATORE DI ROTULA E LCL-LCM TAGLIA XXXL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718350554.
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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