gudid
Primary ID: CUFF-210L
VASOCUFF (UDI CUFF-210L)
Manufactured by NEWMAN MEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VASOCUFF - Primary ID CUFF-210L
Device Regulatory Overview
The VASOCUFF (Model/Catalog Number: CUFF-210L) is a medical device manufactured by NEWMAN MEDICAL LLC. This product is indexed under FDA Product Code / Category Classification DXQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CUFF-210L
- Product Code / EMDN
- DXQ
- Device Name
- Vasocuff Vascular Cuff, 12cm long, for use above knee
- Database Sync Date
- 2026-08-09 09:49:32
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 VASOCUFF?
The registered manufacturer of record for VASOCUFF is NEWMAN MEDICAL LLC.
What is the Primary UDI-DI identifier for VASOCUFF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CUFF-210L.
What classification code is assigned to this device?
This device is registered under product classification code DXQ.
Similar Classification Devices (DXQ)
Other Devices by NEWMAN MEDICAL LLC
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