gudid Primary ID: Intro Pack 75g jar

Spectra Fresh Mint (UDI Intro Pack 75g jar)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spectra Fresh Mint (Model/Catalog Number: Intro Pack 75g jar) is a medical device manufactured by PREVEST DENPRO LIMITED. This product is indexed under FDA Product Code / Category Classification EJR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Intro Pack 75g jar
Product Code / EMDN: EJR
Device Name
Database Sync Date: 2026-08-09 09:01:11

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Spectra Fresh Mint?

The registered manufacturer of record for Spectra Fresh Mint is PREVEST DENPRO LIMITED.

What is the Primary UDI-DI identifier for Spectra Fresh Mint?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Intro Pack 75g jar.

What classification code is assigned to this device?

This device is registered under product classification code EJR.

Similar Classification Devices (EJR)

Other Devices by PREVEST DENPRO LIMITED

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint