eudamed_udi
Primary ID: 10705034214955
VIPER2 SYSTEM (UDI 10705034214955)
Manufactured by Medos International SARL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIPER2 SYSTEM - Primary ID 10705034214955
Device Regulatory Overview
The VIPER2 SYSTEM (Model/Catalog Number: 286760350) is a medical device manufactured by Medos International SARL. This product is indexed under FDA Product Code / Category Classification L091001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 286760350
- Product Code / EMDN
- L091001
- Device Name
- Viper Guide Wire Driver Handle Screw Rod Holder Pin Torque Device Torque Wrench Screw Inserter AWL Tightener Compression/Distration Rack Tab Tab Sleeve Alignment Guide Screw Extension Inserter Rod Rotator Reduction Cap Handle & Nut Tightener
- Database Sync Date
- 2026-08-09 16:29:02
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 VIPER2 SYSTEM?
The registered manufacturer of record for VIPER2 SYSTEM is Medos International SARL.
What is the Primary UDI-DI identifier for VIPER2 SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10705034214955.
What classification code is assigned to this device?
This device is registered under product classification code L091001.
Similar Classification Devices (L091001)
Other Devices by Medos International SARL
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