GUDIDData
eudamed_udi Primary ID: 04560323648519

Applanation Tonometer AT-2 (UDI 04560323648519)

Manufactured by Takagi seiko

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Applanation Tonometer AT-2 - Primary ID 04560323648519

Device Regulatory Overview

The Applanation Tonometer AT-2 (Model/Catalog Number: AT-2) is a medical device manufactured by Takagi seiko. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AT-2
Product Code / EMDN
Q0299
Device Name
Applanation Tonometer
Database Sync Date
2026-08-09 16:45:42

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 Applanation Tonometer AT-2?

The registered manufacturer of record for Applanation Tonometer AT-2 is Takagi seiko.

What is the Primary UDI-DI identifier for Applanation Tonometer AT-2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04560323648519.

What classification code is assigned to this device?

This device is registered under product classification code Q0299.

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