Formaldehyde 4% Q Path / FORMALINE 10% (UDI 07312056209003)
Manufactured by VWR INTERNATIONAL SAS
Device Regulatory Overview
The Formaldehyde 4% Q Path / FORMALINE 10% (Model/Catalog Number: FOR0060AF59001) 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
- FOR0060AF59001
- Product Code / EMDN
- W01030705
- Device Name
- Q Path Fixative Formaldehyde
- Database Sync Date
- 2026-08-09 16:29:44
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 Formaldehyde 4% Q Path / FORMALINE 10%?
The registered manufacturer of record for Formaldehyde 4% Q Path / FORMALINE 10% is VWR INTERNATIONAL SAS.
What is the Primary UDI-DI identifier for Formaldehyde 4% Q Path / FORMALINE 10%?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312056209003.
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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