gudid
Primary ID: 04013500
W&H (UDI 04013500)
Manufactured by NICHROMINOX
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for W&H - Primary ID 04013500
Device Regulatory Overview
The W&H (Model/Catalog Number: 04013500) is a medical device manufactured by NICHROMINOX. This product is indexed under FDA Product Code / Category Classification FSM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04013500
- Product Code / EMDN
- FSM
- Device Name
- STORAGE CASSETTE 28X18 - EMPTY
- Database Sync Date
- 2026-08-09 09:33:54
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of W&H?
The registered manufacturer of record for W&H is NICHROMINOX.
What is the Primary UDI-DI identifier for W&H?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04013500.
What classification code is assigned to this device?
This device is registered under product classification code FSM.
Similar Classification Devices (FSM)
Other Devices by NICHROMINOX
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