ICS Impulse Vision Denied Solution 2 Kit (200 pcs) (UDI 041482)
Manufactured by NATUS MANUFACTURING LIMITED
Device Regulatory Overview
The ICS Impulse Vision Denied Solution 2 Kit (200 pcs) (Model/Catalog Number: 041482) is a medical device manufactured by NATUS MANUFACTURING LIMITED. This product is indexed under FDA Product Code / Category Classification GWN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 041482
- Product Code / EMDN
- GWN
- Device Name
- 1085 ICS Impulse Vision Denied Solution 2 Kit (200 pcs)
- Database Sync Date
- 2026-08-09 09:12:40
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 ICS Impulse Vision Denied Solution 2 Kit (200 pcs)?
The registered manufacturer of record for ICS Impulse Vision Denied Solution 2 Kit (200 pcs) is NATUS MANUFACTURING LIMITED.
What is the Primary UDI-DI identifier for ICS Impulse Vision Denied Solution 2 Kit (200 pcs)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 041482.
What classification code is assigned to this device?
This device is registered under product classification code GWN.
Similar Classification Devices (GWN)
Other Devices by NATUS MANUFACTURING LIMITED
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