eudamed_udi
Primary ID: 07312056569954
Easyfix Q Path (UDI 07312056569954)
Manufactured by VWR INTERNATIONAL SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Easyfix Q Path - Primary ID 07312056569954
Device Regulatory Overview
The Easyfix Q Path (Model/Catalog Number: EAS0061C660003) is a medical device manufactured by VWR INTERNATIONAL SAS. This product is indexed under FDA Product Code / Category Classification W01030705 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EAS0061C660003
- Product Code / EMDN
- W01030705
- Device Name
- Q Path Fixative Cytological
- Database Sync Date
- 2026-08-09 16:49:39
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 Easyfix Q Path?
The registered manufacturer of record for Easyfix Q Path is VWR INTERNATIONAL SAS.
What is the Primary UDI-DI identifier for Easyfix Q Path?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312056569954.
What classification code is assigned to this device?
This device is registered under product classification code W01030705.
Similar Classification Devices (W01030705)
Other Devices by VWR INTERNATIONAL SAS
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