gudid
Primary ID: SUP3018BLK
CoreTech (UDI SUP3018BLK)
Manufactured by VIVE HEALTH LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CoreTech - Primary ID SUP3018BLK
Device Regulatory Overview
The CoreTech (Model/Catalog Number: SUP3018BLK) is a medical device manufactured by VIVE HEALTH LLC. This product is indexed under FDA Product Code / Category Classification IPT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SUP3018BLK
- Product Code / EMDN
- IPT
- Device Name
- 464 TLSO
- 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 CoreTech?
The registered manufacturer of record for CoreTech is VIVE HEALTH LLC.
What is the Primary UDI-DI identifier for CoreTech?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SUP3018BLK.
What classification code is assigned to this device?
This device is registered under product classification code IPT.
Similar Classification Devices (IPT)
Other Devices by VIVE HEALTH LLC
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