eudamed_udi
Primary ID: 03665155001486
ACCESS V2 (UDI 03665155001486)
Manufactured by FDI FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACCESS V2 - Primary ID 03665155001486
Device Regulatory Overview
The ACCESS V2 (Model/Catalog Number: ACV2/02/02) is a medical device manufactured by FDI FRANCE. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACV2/02/02
- Product Code / EMDN
- Y12030601
- Device Name
- Canne anglaise
- Database Sync Date
- 2026-08-09 17:56:56
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 ACCESS V2?
The registered manufacturer of record for ACCESS V2 is FDI FRANCE.
What is the Primary UDI-DI identifier for ACCESS V2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665155001486.
What classification code is assigned to this device?
This device is registered under product classification code Y12030601.
Similar Classification Devices (Y12030601)
Other Devices by FDI FRANCE
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