GUDIDData
eudamed_udi Primary ID: 05604425001311

Unspecified Brand (UDI 05604425001311)

Manufactured by PROHS Equipamento Hospitalar e Serviços Associados S.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 05604425001311

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: FJ 930L 2PD (70*70*190)) is a medical device manufactured by PROHS Equipamento Hospitalar e Serviços Associados S.A.. This product is indexed under FDA Product Code / Category Classification Z12011304 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FJ 930L 2PD (70*70*190)
Product Code / EMDN
Z12011304
Device Name
PROHS Horizontal Steam Sterilizer
Database Sync Date
2026-08-09 16:44:50

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is PROHS Equipamento Hospitalar e Serviços Associados S.A..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05604425001311.

What classification code is assigned to this device?

This device is registered under product classification code Z12011304.

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