gudid
Primary ID: 1202-02
Capture (UDI 1202-02)
Manufactured by DIVERSATEK HEALTHCARE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Capture - Primary ID 1202-02
Device Regulatory Overview
The Capture (Model/Catalog Number: 1202-02) is a medical device manufactured by DIVERSATEK HEALTHCARE, INC.. This product is indexed under FDA Product Code / Category Classification CBC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1202-02
- Product Code / EMDN
- CBC
- Device Name
- 2-Tray Polyp Trap
- Database Sync Date
- 2026-08-09 09:31:28
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 Capture?
The registered manufacturer of record for Capture is DIVERSATEK HEALTHCARE, INC..
What is the Primary UDI-DI identifier for Capture?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1202-02.
What classification code is assigned to this device?
This device is registered under product classification code CBC.
Similar Classification Devices (CBC)
Other Devices by DIVERSATEK HEALTHCARE, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint