VAE-Extraction Solution with Internal Standards (UDI 06438172404113)
Manufactured by Labsystems Diagnostics Oy
Device Regulatory Overview
The VAE-Extraction Solution with Internal Standards (Model/Catalog Number: 3469880) is a medical device manufactured by Labsystems Diagnostics Oy. This product is indexed under FDA Product Code / Category Classification W0102152206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3469880
- Product Code / EMDN
- W0102152206
- Device Name
- VAE-Extraction Solution with Internal Standards
- Database Sync Date
- 2026-08-09 17:55:52
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 VAE-Extraction Solution with Internal Standards?
The registered manufacturer of record for VAE-Extraction Solution with Internal Standards is Labsystems Diagnostics Oy.
What is the Primary UDI-DI identifier for VAE-Extraction Solution with Internal Standards?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438172404113.
What classification code is assigned to this device?
This device is registered under product classification code W0102152206.
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Other Devices by Labsystems Diagnostics Oy
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