LT (UDI 06976714790329)
Manufactured by Linfen Houma Economic Development Zone Yongxing Medical Device Co.,Ltd
Device Regulatory Overview
The LT (Model/Catalog Number: Superfluid) is a medical device manufactured by Linfen Houma Economic Development Zone Yongxing Medical Device Co.,Ltd. This product is indexed under FDA Product Code / Category Classification M04040702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Superfluid
- Product Code / EMDN
- M04040702
- Device Name
- Silicone rubber copy material
- Database Sync Date
- 2026-08-09 16:29:21
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 LT?
The registered manufacturer of record for LT is Linfen Houma Economic Development Zone Yongxing Medical Device Co.,Ltd.
What is the Primary UDI-DI identifier for LT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976714790329.
What classification code is assigned to this device?
This device is registered under product classification code M04040702.
Similar Classification Devices (M04040702)
Other Devices by Linfen Houma Economic Development Zone Yongxing Medical Device Co.,Ltd
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