Rapid Ketamine Test Strip (UDI 06921963710147)
Manufactured by Xiamen Boson Biotech Co., Ltd.
Device Regulatory Overview
The Rapid Ketamine Test Strip (Model/Catalog Number: 1L07S3) is a medical device manufactured by Xiamen Boson Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1L07S3
- Product Code / EMDN
- W0102160599
- Device Name
- Rapid Ketamine Test Strip
- Database Sync Date
- 2026-08-09 16:46:56
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 Rapid Ketamine Test Strip?
The registered manufacturer of record for Rapid Ketamine Test Strip is Xiamen Boson Biotech Co., Ltd..
What is the Primary UDI-DI identifier for Rapid Ketamine Test Strip?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921963710147.
What classification code is assigned to this device?
This device is registered under product classification code W0102160599.
Similar Classification Devices (W0102160599)
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