SEQUAhold WOUND CLOSURE DEVICE (UDI LKB1002)
Manufactured by Foshan United Medical Technologies Ltd.
Device Regulatory Overview
The SEQUAhold WOUND CLOSURE DEVICE (Model/Catalog Number: LKB1002) is a medical device manufactured by Foshan United Medical Technologies Ltd.. This product is indexed under FDA Product Code / Category Classification MGO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LKB1002
- Product Code / EMDN
- MGO
- Device Name
- Database Sync Date
- 2026-08-09 09:24:51
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 SEQUAhold WOUND CLOSURE DEVICE?
The registered manufacturer of record for SEQUAhold WOUND CLOSURE DEVICE is Foshan United Medical Technologies Ltd..
What is the Primary UDI-DI identifier for SEQUAhold WOUND CLOSURE DEVICE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LKB1002.
What classification code is assigned to this device?
This device is registered under product classification code MGO.
Similar Classification Devices (MGO)
Other Devices by Foshan United Medical Technologies Ltd.
Programmatic Export
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