INSTI HIV-1/HIV-2 Control Test Kit (UDI 90-1031)
Manufactured by Biolytical Laboratories Inc
Device Regulatory Overview
The INSTI HIV-1/HIV-2 Control Test Kit (Model/Catalog Number: 90-1031) is a medical device manufactured by Biolytical Laboratories Inc. This product is indexed under FDA Product Code / Category Classification MZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90-1031
- Product Code / EMDN
- MZF
- Device Name
- INSTI HIV-1/HIV-2 Control Test Kit
- Database Sync Date
- 2026-08-09 09:04:23
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 INSTI HIV-1/HIV-2 Control Test Kit?
The registered manufacturer of record for INSTI HIV-1/HIV-2 Control Test Kit is Biolytical Laboratories Inc.
What is the Primary UDI-DI identifier for INSTI HIV-1/HIV-2 Control Test Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90-1031.
What classification code is assigned to this device?
This device is registered under product classification code MZF.
Similar Classification Devices (MZF)
Other Devices by Biolytical Laboratories Inc
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