GUDIDData
gudid Primary ID: C121-2021

Mission Cholesterol Optical Check Device (UDI C121-2021)

Manufactured by Acon Laboratories, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mission Cholesterol Optical Check Device - Primary ID C121-2021

Device Regulatory Overview

The Mission Cholesterol Optical Check Device (Model/Catalog Number: C121-2021) is a medical device manufactured by Acon Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification JGY 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-2322-2015 View Full Alert →

Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Blow bags included Product Usage: The Breath Alcohol Detector is for the...

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Technical Specifications

Model Number
C121-2021
Product Code / EMDN
JGY
Device Name
Meter optics checker
Database Sync Date
2026-08-09 09:17:18

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 Mission Cholesterol Optical Check Device?

The registered manufacturer of record for Mission Cholesterol Optical Check Device is Acon Laboratories, Inc..

What is the Primary UDI-DI identifier for Mission Cholesterol Optical Check Device?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C121-2021.

What classification code is assigned to this device?

This device is registered under product classification code JGY.

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