eudamed_udi
Primary ID: 08056045431455
GINOCCHIERA ELASTICA (UDI 08056045431455)
Manufactured by SAFTE S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GINOCCHIERA ELASTICA - Primary ID 08056045431455
Device Regulatory Overview
The GINOCCHIERA ELASTICA (Model/Catalog Number: 403BGMD) is a medical device manufactured by SAFTE S.r.l.. This product is indexed under FDA Product Code / Category Classification M030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 403BGMD
- Product Code / EMDN
- M030499
- Device Name
- ORTESI
- Database Sync Date
- 2026-08-09 16:28:48
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 GINOCCHIERA ELASTICA?
The registered manufacturer of record for GINOCCHIERA ELASTICA is SAFTE S.r.l..
What is the Primary UDI-DI identifier for GINOCCHIERA ELASTICA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056045431455.
What classification code is assigned to this device?
This device is registered under product classification code M030499.
Similar Classification Devices (M030499)
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