gudid Primary ID: 60620115

AH PLUS JET (UDI 60620115)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AH PLUS JET (Model/Catalog Number: 60620115) is a medical device manufactured by Dentsply De Trey GmbH. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 60620115
Product Code / EMDN: KIF
Device Name: AH Plus Jet Starter Kit is a 2 component paste/paste root canal sealer based on epoxy-amine resin. AH Plus Jet is received in a syringe (D010K3001600) delivery for homogeneous mixing of both pastes. With its supporting accessories (Mixing/Intraoral Tips, Mixing Pad and Organizer Tray) it can be classified as a convenience kit.
Database Sync Date: 2026-08-09 09:02:02

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 AH PLUS JET?

The registered manufacturer of record for AH PLUS JET is Dentsply De Trey GmbH.

What is the Primary UDI-DI identifier for AH PLUS JET?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60620115.

What classification code is assigned to this device?

This device is registered under product classification code KIF.

Similar Classification Devices (KIF)

Other Devices by Dentsply De Trey GmbH

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