gudid
Primary ID: NTC023IB-VST12
Neotech Care (UDI NTC023IB-VST12)
Manufactured by NEOTECH CARE INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neotech Care - Primary ID NTC023IB-VST12
Device Regulatory Overview
The Neotech Care (Model/Catalog Number: NTC023IB-VST12) is a medical device manufactured by NEOTECH CARE INC.. This product is indexed under FDA Product Code / Category Classification KYR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NTC023IB-VST12
- Product Code / EMDN
- KYR
- Device Name
- Database Sync Date
- 2026-08-09 09:59:39
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Neotech Care?
The registered manufacturer of record for Neotech Care is NEOTECH CARE INC..
What is the Primary UDI-DI identifier for Neotech Care?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NTC023IB-VST12.
What classification code is assigned to this device?
This device is registered under product classification code KYR.
Similar Classification Devices (KYR)
Other Devices by NEOTECH CARE INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint