DCK-A004-10030 (UDI 06978111927735)
Manufactured by Promisemed Hangzhou Meditech Co., Ltd.
Device Regulatory Overview
The DCK-A004-10030 (Model/Catalog Number: VeriEcto) is a medical device manufactured by Promisemed Hangzhou Meditech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A060201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VeriEcto
- Product Code / EMDN
- A060201
- Device Name
- Multipurpose Drainage Catheters
- Database Sync Date
- 2026-08-09 17:09:48
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 DCK-A004-10030?
The registered manufacturer of record for DCK-A004-10030 is Promisemed Hangzhou Meditech Co., Ltd..
What is the Primary UDI-DI identifier for DCK-A004-10030?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978111927735.
What classification code is assigned to this device?
This device is registered under product classification code A060201.
Similar Classification Devices (A060201)
Other Devices by Promisemed Hangzhou Meditech Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint