Tuberculosis Antibody Rapid Test (UDI 06974566302820)
Manufactured by Zhuhai Encode Medical Engineering Co., Ltd.
Device Regulatory Overview
The Tuberculosis Antibody Rapid Test (Model/Catalog Number: ITA-812) is a medical device manufactured by Zhuhai Encode Medical Engineering Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105010702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ITA-812
- Product Code / EMDN
- W0105010702
- Device Name
- Tuberculosis Antibody Rapid Test
- Database Sync Date
- 2026-08-09 16:28:54
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 Tuberculosis Antibody Rapid Test?
The registered manufacturer of record for Tuberculosis Antibody Rapid Test is Zhuhai Encode Medical Engineering Co., Ltd..
What is the Primary UDI-DI identifier for Tuberculosis Antibody Rapid Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974566302820.
What classification code is assigned to this device?
This device is registered under product classification code W0105010702.
Similar Classification Devices (W0105010702)
Other Devices by Zhuhai Encode Medical Engineering Co., Ltd.
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