eudamed_udi
Primary ID: 03701475323515
NICHROMINOX (UDI 03701475323515)
Manufactured by NICHROMINOX
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NICHROMINOX - Primary ID 03701475323515
Device Regulatory Overview
The NICHROMINOX (Model/Catalog Number: PN300350-5) is a medical device manufactured by NICHROMINOX. This product is indexed under FDA Product Code / Category Classification S010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PN300350-5
- Product Code / EMDN
- S010499
- Device Name
- ALUMINIUM INSTRUMENT HOLDERS
- Database Sync Date
- 2026-08-09 16:28:48
Full Regulatory Attributes
π Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 03701475323515.
What classification code is assigned to this device?
This device is registered under product classification code S010499.
Similar Classification Devices (S010499)
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