gudid
Primary ID: CU-US3860HP
AMC (UDI CU-US3860HP)
Manufactured by LifeSync Corporation
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMC - Primary ID CU-US3860HP
Device Regulatory Overview
The AMC (Model/Catalog Number: CU-US3860HP) is a medical device manufactured by LifeSync Corporation. This product is indexed under FDA Product Code / Category Classification DXQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CU-US3860HP
- Product Code / EMDN
- DXQ
- Device Name
- Reusable Cuff, Single Tube, Lg Adult/Thigh, HP Fitting
- Database Sync Date
- 2026-08-09 09:35:45
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 AMC?
The registered manufacturer of record for AMC is LifeSync Corporation.
What is the Primary UDI-DI identifier for AMC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CU-US3860HP.
What classification code is assigned to this device?
This device is registered under product classification code DXQ.
Similar Classification Devices (DXQ)
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