Multi-Drugs Rapid Test Device (UDI 06976202761886)
Manufactured by Zhejiang Greylynx Biotech Co., Ltd.
Device Regulatory Overview
The Multi-Drugs Rapid Test Device (Model/Catalog Number: VDOA-253-001) is a medical device manufactured by Zhejiang Greylynx Biotech 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
- VDOA-253-001
- Product Code / EMDN
- W0102160511
- Device Name
- Multi-Drugs Rapid Test Device
- Database Sync Date
- 2026-08-09 16:29:44
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 Multi-Drugs Rapid Test Device?
The registered manufacturer of record for Multi-Drugs Rapid Test Device is Zhejiang Greylynx Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Multi-Drugs Rapid Test Device?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976202761886.
What classification code is assigned to this device?
This device is registered under product classification code W0102160511.
Similar Classification Devices (W0102160511)
Other Devices by Zhejiang Greylynx Biotech Co., Ltd.
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