Unspecified Brand (UDI D-A064D9)
Manufactured by Phase Scientific International Limited
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: INDICAID™ Multi drug Rapid Test) is a medical device manufactured by Phase Scientific International Limited. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INDICAID™ Multi drug Rapid Test
- Product Code / EMDN
- W0102160511
- Device Name
- INDICAID™ Multi drug Rapid Test
- Database Sync Date
- 2026-08-09 16:30:11
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Phase Scientific International Limited.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-A064D9.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
Other Devices by Phase Scientific International Limited
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