gudid
Primary ID: AD32010
Topex (UDI AD32010)
Manufactured by Sultan Healthcare Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Topex - Primary ID AD32010
Device Regulatory Overview
The Topex (Model/Catalog Number: AD32010) is a medical device manufactured by Sultan Healthcare Inc. This product is indexed under FDA Product Code / Category Classification KMT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AD32010
- Product Code / EMDN
- KMT
- Device Name
- Topex Dual Arch Tray Pedo Bag of 50
- Database Sync Date
- 2026-08-09 09:03:02
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 Topex?
The registered manufacturer of record for Topex is Sultan Healthcare Inc.
What is the Primary UDI-DI identifier for Topex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AD32010.
What classification code is assigned to this device?
This device is registered under product classification code KMT.
Similar Classification Devices (KMT)
Other Devices by Sultan Healthcare Inc
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint