GUDIDData
eudamed_udi Primary ID: 03701475318948

NICHROMINOX (UDI 03701475318948)

Manufactured by NICHROMINOX

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NICHROMINOX - Primary ID 03701475318948

Device Regulatory Overview

The NICHROMINOX (Model/Catalog Number: PN091500) is a medical device manufactured by NICHROMINOX. This product is indexed under FDA Product Code / Category Classification M040299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PN091500
Product Code / EMDN
M040299
Device Name
COMPRESSE OROPHARYNGÉE
Database Sync Date
2026-08-09 17:03:08

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 NICHROMINOX?

The registered manufacturer of record for NICHROMINOX is NICHROMINOX.

What is the Primary UDI-DI identifier for NICHROMINOX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701475318948.

What classification code is assigned to this device?

This device is registered under product classification code M040299.

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