eudamed_udi
Primary ID: 06970581430944
Accu-Tell® BAR Strip (Urine) (UDI 06970581430944)
Manufactured by AccuBioTech Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Accu-Tell® BAR Strip (Urine) - Primary ID 06970581430944
Device Regulatory Overview
The Accu-Tell® BAR Strip (Urine) (Model/Catalog Number: ABT-DOA-A28) is a medical device manufactured by AccuBioTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ABT-DOA-A28
- Product Code / EMDN
- W0102160503
- Device Name
- Accu-Tell® BAR Test
- Database Sync Date
- 2026-08-09 16:30:30
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® BAR Strip (Urine)?
The registered manufacturer of record for Accu-Tell® BAR Strip (Urine) is AccuBioTech Co., Ltd..
What is the Primary UDI-DI identifier for Accu-Tell® BAR Strip (Urine)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970581430944.
What classification code is assigned to this device?
This device is registered under product classification code W0102160503.
Similar Classification Devices (W0102160503)
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