eudamed_udi
Primary ID: 07312056614661
Eosin Y alcoholic 0,2% Q Path (UDI 07312056614661)
Manufactured by VWR INTERNATIONAL SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Eosin Y alcoholic 0,2% Q Path - Primary ID 07312056614661
Device Regulatory Overview
The Eosin Y alcoholic 0,2% Q Path (Model/Catalog Number: 10047003.) is a medical device manufactured by VWR INTERNATIONAL SAS. This product is indexed under FDA Product Code / Category Classification W01030708 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10047003.
- Product Code / EMDN
- W01030708
- Device Name
- Q Path Staining Solution
- Database Sync Date
- 2026-08-09 16:51:16
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 Eosin Y alcoholic 0,2% Q Path?
The registered manufacturer of record for Eosin Y alcoholic 0,2% Q Path is VWR INTERNATIONAL SAS.
What is the Primary UDI-DI identifier for Eosin Y alcoholic 0,2% Q Path?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312056614661.
What classification code is assigned to this device?
This device is registered under product classification code W01030708.
Similar Classification Devices (W01030708)
Other Devices by VWR INTERNATIONAL SAS
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