eudamed_udi Primary ID: 06921756471095

On Call (UDI 06921756471095)

Manufactured by Acon Biotech (Hangzhou) Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The On Call (Model/Catalog Number: G123-311-201) is a medical device manufactured by Acon Biotech (Hangzhou) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W010106010801 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0945-2022 View Full Alert →

Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing), CE marked...

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Technical Specifications

Model Number: G123-311-201
Product Code / EMDN: W010106010801
Device Name: On Call Plus Glucose Control Solution
Database Sync Date: 2026-08-09 16:29:57

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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Frequently Asked Questions

Who is the primary manufacturer of On Call?

The registered manufacturer of record for On Call is Acon Biotech (Hangzhou) Co., Ltd..

What is the Primary UDI-DI identifier for On Call?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06921756471095.

What classification code is assigned to this device?

This device is registered under product classification code W010106010801.

Similar Classification Devices (W010106010801)

Other Devices by Acon Biotech (Hangzhou) Co., Ltd.

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