eudamed_udi
Primary ID: 08028718515526
IMMOBILIZZATORE DI GOMITO SINISTRO L (UDI 08028718515526)
Manufactured by PAVIS SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IMMOBILIZZATORE DI GOMITO SINISTRO L - Primary ID 08028718515526
Device Regulatory Overview
The IMMOBILIZZATORE DI GOMITO SINISTRO L (Model/Catalog Number: 138 BL SX L) is a medical device manufactured by PAVIS SPA. This product is indexed under FDA Product Code / Category Classification Y060615 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 138 BL SX L
- Product Code / EMDN
- Y060615
- Device Name
- LINEA MANO BRACCIO POLSO
- Database Sync Date
- 2026-08-09 16:51:39
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 IMMOBILIZZATORE DI GOMITO SINISTRO L?
The registered manufacturer of record for IMMOBILIZZATORE DI GOMITO SINISTRO L is PAVIS SPA.
What is the Primary UDI-DI identifier for IMMOBILIZZATORE DI GOMITO SINISTRO L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718515526.
What classification code is assigned to this device?
This device is registered under product classification code Y060615.
Similar Classification Devices (Y060615)
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