eudamed_udi
Primary ID: 08056045435989
ORTESI PER L'IMMOBILIZZAZIONE DEL POLLICE (UDI 08056045435989)
Manufactured by SAFTE S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORTESI PER L'IMMOBILIZZAZIONE DEL POLLICE - Primary ID 08056045435989
Device Regulatory Overview
The ORTESI PER L'IMMOBILIZZAZIONE DEL POLLICE (Model/Catalog Number: 241BGSMD) is a medical device manufactured by SAFTE S.r.l.. This product is indexed under FDA Product Code / Category Classification Y060603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 241BGSMD
- Product Code / EMDN
- Y060603
- Device Name
- ORTESI
- Database Sync Date
- 2026-08-09 16:30:06
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 ORTESI PER L'IMMOBILIZZAZIONE DEL POLLICE?
The registered manufacturer of record for ORTESI PER L'IMMOBILIZZAZIONE DEL POLLICE is SAFTE S.r.l..
What is the Primary UDI-DI identifier for ORTESI PER L'IMMOBILIZZAZIONE DEL POLLICE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056045435989.
What classification code is assigned to this device?
This device is registered under product classification code Y060603.
Similar Classification Devices (Y060603)
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