eudamed_udi
Primary ID: 03700434023275
Tornier Flex Shoulder System (UDI 03700434023275)
Manufactured by Tornier SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tornier Flex Shoulder System - Primary ID 03700434023275
Device Regulatory Overview
The Tornier Flex Shoulder System (Model/Catalog Number: NCR135) is a medical device manufactured by Tornier SAS. This product is indexed under FDA Product Code / Category Classification V0402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NCR135
- Product Code / EMDN
- V0402
- Device Name
- TORNIER SAS CLASS I DEVICES - TRAYS AND TRAY ACCESSORIES - CLASS I - NON STERILE
- Database Sync Date
- 2026-08-09 16:29:03
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 Tornier Flex Shoulder System?
The registered manufacturer of record for Tornier Flex Shoulder System is Tornier SAS.
What is the Primary UDI-DI identifier for Tornier Flex Shoulder System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700434023275.
What classification code is assigned to this device?
This device is registered under product classification code V0402.
Similar Classification Devices (V0402)
Other Devices by Tornier SAS
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