Unspecified Brand (UDI 06970952649500)
Manufactured by Jiangsu Kehua Medical Instrument Technology Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: EDTAK2) is a medical device manufactured by Jiangsu Kehua Medical Instrument Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0503020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EDTAK2
- Product Code / EMDN
- W0503020199
- Device Name
- Disposable transfer pipette(Capillary pipette/Glass capillary tube/Fixed volume pipette/Capillary blood collector)
- Database Sync Date
- 2026-08-09 17:44:37
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 Jiangsu Kehua Medical Instrument Technology 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 06970952649500.
What classification code is assigned to this device?
This device is registered under product classification code W0503020199.
Similar Classification Devices (W0503020199)
Other Devices by Jiangsu Kehua Medical Instrument Technology Co., Ltd.
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