gudid
Primary ID: CR2-LF13W-2QFQF
Amico Diagnostic Cuff (UDI CR2-LF13W-2QFQF)
Manufactured by Amico Diagnostic Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Amico Diagnostic Cuff - Primary ID CR2-LF13W-2QFQF
Device Regulatory Overview
The Amico Diagnostic Cuff (Model/Catalog Number: CR2-LF13W-2QFQF) is a medical device manufactured by Amico Diagnostic Incorporated. This product is indexed under FDA Product Code / Category Classification DXQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CR2-LF13W-2QFQF
- Product Code / EMDN
- DXQ
- Device Name
- Thigh 2-Piece Cuff, 2 Tubes LF, Brown, Submin Female x Submin Female Conn
- Database Sync Date
- 2026-08-09 09:04:19
Full Regulatory Attributes
🔒 Token Gated
{
"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 Amico Diagnostic Cuff?
The registered manufacturer of record for Amico Diagnostic Cuff is Amico Diagnostic Incorporated.
What is the Primary UDI-DI identifier for Amico Diagnostic Cuff?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CR2-LF13W-2QFQF.
What classification code is assigned to this device?
This device is registered under product classification code DXQ.
Similar Classification Devices (DXQ)
Other Devices by Amico Diagnostic Incorporated
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