gudid
Primary ID: SNMR-035-030-2220
VISICOIL MR (UDI SNMR-035-030-2220)
Manufactured by Izi Medical Products, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VISICOIL MR - Primary ID SNMR-035-030-2220
Device Regulatory Overview
The VISICOIL MR (Model/Catalog Number: SNMR-035-030-2220) is a medical device manufactured by Izi Medical Products, LLC. This product is indexed under FDA Product Code / Category Classification IYE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SNMR-035-030-2220
- Product Code / EMDN
- IYE
- Device Name
- 0.35mm x 3.0cm VISICOIL MR Platinum loaded in an 22 gauge 20cm pre-waxed needle.
- Database Sync Date
- 2026-08-09 09:06:21
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 VISICOIL MR?
The registered manufacturer of record for VISICOIL MR is Izi Medical Products, LLC.
What is the Primary UDI-DI identifier for VISICOIL MR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SNMR-035-030-2220.
What classification code is assigned to this device?
This device is registered under product classification code IYE.
Similar Classification Devices (IYE)
Other Devices by Izi Medical Products, LLC
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