Accu-Tell® Multi-9 Drug Panel (Urine) (UDI 06970581431347)
Manufactured by AccuBioTech Co., Ltd.
Device Regulatory Overview
The Accu-Tell® Multi-9 Drug Panel (Urine) (Model/Catalog Number: ABT-DOA-E75) is a medical device manufactured by AccuBioTech 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
- ABT-DOA-E75
- Product Code / EMDN
- W0102160511
- Device Name
- Accu-Tell® Multi-9 Drug Panel (Urine)
- Database Sync Date
- 2026-08-09 16:49:46
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 Accu-Tell® Multi-9 Drug Panel (Urine)?
The registered manufacturer of record for Accu-Tell® Multi-9 Drug Panel (Urine) is AccuBioTech Co., Ltd..
What is the Primary UDI-DI identifier for Accu-Tell® Multi-9 Drug Panel (Urine)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970581431347.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
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