Gonorrhea + Chlamydia Antigen Combo Test Cassette (UDI 06974566302363)
Manufactured by Zhuhai Encode Medical Engineering Co., Ltd.
Device Regulatory Overview
The Gonorrhea + Chlamydia Antigen Combo Test Cassette (Model/Catalog Number: SGC-52225) is a medical device manufactured by Zhuhai Encode Medical Engineering Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105090199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SGC-52225
- Product Code / EMDN
- W0105090199
- Device Name
- Gonorrhea + Chlamydia Antigen Combo Test Cassette
- Database Sync Date
- 2026-08-09 16:29:57
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 Gonorrhea + Chlamydia Antigen Combo Test Cassette?
The registered manufacturer of record for Gonorrhea + Chlamydia Antigen Combo Test Cassette is Zhuhai Encode Medical Engineering Co., Ltd..
What is the Primary UDI-DI identifier for Gonorrhea + Chlamydia Antigen Combo Test Cassette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974566302363.
What classification code is assigned to this device?
This device is registered under product classification code W0105090199.
Similar Classification Devices (W0105090199)
Other Devices by Zhuhai Encode Medical Engineering Co., Ltd.
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