Accu-Tell® Multi-Drug 2 Midstream Pro (Saliva) (UDI D-ABT-DOA-T142U3)
Manufactured by AccuBioTech Co., Ltd.
Device Regulatory Overview
The Accu-Tell® Multi-Drug 2 Midstream Pro (Saliva) (Model/Catalog Number: ABT-DOA-T142) 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-T142
- Product Code / EMDN
- W0102160511
- Device Name
- Accu-Tell® Multi-Drug 2 Midstream Pro (Saliva)
- Database Sync Date
- 2026-08-09 16:50:52
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 Accu-Tell® Multi-Drug 2 Midstream Pro (Saliva)?
The registered manufacturer of record for Accu-Tell® Multi-Drug 2 Midstream Pro (Saliva) is AccuBioTech Co., Ltd..
What is the Primary UDI-DI identifier for Accu-Tell® Multi-Drug 2 Midstream Pro (Saliva)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ABT-DOA-T142U3.
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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