eudamed_udi
Primary ID: 08906030752495
Prowayext (UDI 08906030752495)
Manufactured by Lars Medicare Pvt Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Prowayext - Primary ID 08906030752495
Device Regulatory Overview
The Prowayext (Model/Catalog Number: 2916.00) is a medical device manufactured by Lars Medicare Pvt Ltd. This product is indexed under FDA Product Code / Category Classification A03020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2916.00
- Product Code / EMDN
- A03020199
- Device Name
- 3 - Way Stop Cock With Extension Tube
- Database Sync Date
- 2026-08-09 16:28:52
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 Prowayext?
The registered manufacturer of record for Prowayext is Lars Medicare Pvt Ltd.
What is the Primary UDI-DI identifier for Prowayext?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906030752495.
What classification code is assigned to this device?
This device is registered under product classification code A03020199.
Similar Classification Devices (A03020199)
Other Devices by Lars Medicare Pvt Ltd
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