gudid Primary ID: 299-3

Chrono-log (UDI 299-3)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Chrono-log (Model/Catalog Number: 299-3) is a medical device manufactured by CHRONO-LOG CORP. This product is indexed under FDA Product Code / Category Classification GGP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 299-3
Product Code / EMDN: GGP
Device Name: vW Reference Plasma Normal
Database Sync Date: 2026-08-09 09:22:15

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 Chrono-log?

The registered manufacturer of record for Chrono-log is CHRONO-LOG CORP.

What is the Primary UDI-DI identifier for Chrono-log?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 299-3.

What classification code is assigned to this device?

This device is registered under product classification code GGP.

Similar Classification Devices (GGP)

Other Devices by CHRONO-LOG CORP

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