Multi- Drug Rapid Test (UDI 06936983160735)
Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.
Device Regulatory Overview
The Multi- Drug Rapid Test (Model/Catalog Number: DOA-N154-045J) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160511 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DOA-N154-045J
- Product Code / EMDN
- W0102160511
- Device Name
- Multi- Drug Rapid Test
- Database Sync Date
- 2026-08-09 16:29:34
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 Multi- Drug Rapid Test?
The registered manufacturer of record for Multi- Drug Rapid Test is Hangzhou Alltest Biotech.Co.,Ltd..
What is the Primary UDI-DI identifier for Multi- Drug Rapid Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936983160735.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
Other Devices by Hangzhou Alltest Biotech.Co.,Ltd.
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