Q Path Containers 150 mL Blue cap (UDI 07312056588443)
Manufactured by VWR INTERNATIONAL SAS
Device Regulatory Overview
The Q Path Containers 150 mL Blue cap (Model/Catalog Number: 216-1319) is a medical device manufactured by VWR INTERNATIONAL SAS. This product is indexed under FDA Product Code / Category Classification W05020103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 216-1319
- Product Code / EMDN
- W05020103
- Device Name
- Q Path Specimen Container
- Database Sync Date
- 2026-08-09 16:47:01
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 Containers 150 mL Blue cap?
The registered manufacturer of record for Q Path Containers 150 mL Blue cap is VWR INTERNATIONAL SAS.
What is the Primary UDI-DI identifier for Q Path Containers 150 mL Blue cap?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07312056588443.
What classification code is assigned to this device?
This device is registered under product classification code W05020103.
Similar Classification Devices (W05020103)
Other Devices by VWR INTERNATIONAL SAS
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