GUDIDData
gudid Primary ID: Pressure Cuff Size 10

Pressure Cuff Size 10 (UDI Pressure Cuff Size 10)

Manufactured by VIASONIX LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pressure Cuff Size 10 - Primary ID Pressure Cuff Size 10

Device Regulatory Overview

The Pressure Cuff Size 10 (Model/Catalog Number: Pressure Cuff Size 10) is a medical device manufactured by VIASONIX LTD. This product is indexed under FDA Product Code / Category Classification JOP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Pressure Cuff Size 10
Product Code / EMDN
JOP
Device Name
The intended use of the pressure cuffs is to measure non-invasively blood pressure
Database Sync Date
2026-08-09 09:18:18

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Pressure Cuff Size 10?

The registered manufacturer of record for Pressure Cuff Size 10 is VIASONIX LTD.

What is the Primary UDI-DI identifier for Pressure Cuff Size 10?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Pressure Cuff Size 10.

What classification code is assigned to this device?

This device is registered under product classification code JOP.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint