GUDIDData
eudamed_udi Primary ID: 04719883630285

MEDI FUSOR overtrycksmanschett (UDI 04719883630285)

Manufactured by Pacific Hospital Supply Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDI FUSOR overtrycksmanschett - Primary ID 04719883630285

Device Regulatory Overview

The MEDI FUSOR overtrycksmanschett (Model/Catalog Number: 604807) is a medical device manufactured by Pacific Hospital Supply Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12030399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
604807
Product Code / EMDN
Z12030399
Device Name
Pressure Infusion Bag
Database Sync Date
2026-08-09 16:44:57

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 MEDI FUSOR overtrycksmanschett?

The registered manufacturer of record for MEDI FUSOR overtrycksmanschett is Pacific Hospital Supply Co., Ltd..

What is the Primary UDI-DI identifier for MEDI FUSOR overtrycksmanschett?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719883630285.

What classification code is assigned to this device?

This device is registered under product classification code Z12030399.

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