gudid
Primary ID: SUP3044BLK35
Vive (UDI SUP3044BLK35)
Manufactured by VIVE HEALTH LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vive - Primary ID SUP3044BLK35
Device Regulatory Overview
The Vive (Model/Catalog Number: SUP3044BLK35) is a medical device manufactured by VIVE HEALTH LLC. This product is indexed under FDA Product Code / Category Classification IQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SUP3044BLK35
- Product Code / EMDN
- IQK
- Device Name
- Neck Support Brace (3.5")
- Database Sync Date
- 2026-08-09 09:12:30
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 Vive?
The registered manufacturer of record for Vive is VIVE HEALTH LLC.
What is the Primary UDI-DI identifier for Vive?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SUP3044BLK35.
What classification code is assigned to this device?
This device is registered under product classification code IQK.
Similar Classification Devices (IQK)
Other Devices by VIVE HEALTH LLC
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