gudid Primary ID: VC-701

Cliq Aspirator (UDI VC-701)

Manufactured by ANEST IWATA SPARMAX Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Cliq Aspirator (Model/Catalog Number: VC-701) is a medical device manufactured by ANEST IWATA SPARMAX Co., Ltd.. This product is indexed under FDA Product Code / Category Classification JCX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VC-701
Product Code / EMDN: JCX
Device Name: Aspirator, Powered Suction Pump.
Database Sync Date: 2026-08-09 09:15:30

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 Cliq Aspirator?

The registered manufacturer of record for Cliq Aspirator is ANEST IWATA SPARMAX Co., Ltd..

What is the Primary UDI-DI identifier for Cliq Aspirator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VC-701.

What classification code is assigned to this device?

This device is registered under product classification code JCX.

Similar Classification Devices (JCX)

Other Devices by ANEST IWATA SPARMAX Co., Ltd.

Programmatic Export

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

JSON API Endpoint