Unspecified Brand (UDI 06977903344422)
Manufactured by GeneSign Biotech (Xiamen)Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: GS110708C25) is a medical device manufactured by GeneSign Biotech (Xiamen)Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105041001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS110708C25
- Product Code / EMDN
- W0105041001
- Device Name
- HPV L1/E7 Antigen Rapid Test
- Database Sync Date
- 2026-08-09 16:29:06
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is GeneSign Biotech (Xiamen)Co., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977903344422.
What classification code is assigned to this device?
This device is registered under product classification code W0105041001.
Similar Classification Devices (W0105041001)
Other Devices by GeneSign Biotech (Xiamen)Co., Ltd.
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