eudamed_udi Primary ID: 03700735617357

PE PLAST STERIBLUE (UDI 03700735617357)

Manufactured by MEDISTOCK

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PE PLAST STERIBLUE (Model/Catalog Number: SB-PLTRAY-HL-1) is a medical device manufactured by MEDISTOCK. This product is indexed under FDA Product Code / Category Classification Q010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SB-PLTRAY-HL-1
Product Code / EMDN: Q010402
Device Name: PORTE EMPREINTE
Database Sync Date: 2026-08-09 16:29:05

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 PE PLAST STERIBLUE?

The registered manufacturer of record for PE PLAST STERIBLUE is MEDISTOCK.

What is the Primary UDI-DI identifier for PE PLAST STERIBLUE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700735617357.

What classification code is assigned to this device?

This device is registered under product classification code Q010402.

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