eudamed_udi
Primary ID: 07312056606260
Q Path Microtwin (UDI 07312056606260)
Manufactured by VWR INTERNATIONAL SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Q Path Microtwin - Primary ID 07312056606260
Device Regulatory Overview
The Q Path Microtwin (Model/Catalog Number: 720-2188) is a medical device manufactured by VWR INTERNATIONAL SAS. This product is indexed under FDA Product Code / Category Classification W05030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 720-2188
- Product Code / EMDN
- W05030501
- Device Name
- Q Path Cassette
- Database Sync Date
- 2026-08-09 16:48:38
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 Q Path Microtwin?
The registered manufacturer of record for Q Path Microtwin is VWR INTERNATIONAL SAS.
What is the Primary UDI-DI identifier for Q Path Microtwin?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312056606260.
What classification code is assigned to this device?
This device is registered under product classification code W05030501.
Similar Classification Devices (W05030501)
Other Devices by VWR INTERNATIONAL SAS
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