SEESHEEN (UDI 06970680130073)
Manufactured by Zhuhai Seesheen Medical Technology Co., Ltd.
Device Regulatory Overview
The SEESHEEN (Model/Catalog Number: EN-1039) is a medical device manufactured by Zhuhai Seesheen Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12021006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EN-1039
- Product Code / EMDN
- Z12021006
- Device Name
- Flexible video rhinolaryngoscope
- Database Sync Date
- 2026-08-09 16:29:04
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 SEESHEEN?
The registered manufacturer of record for SEESHEEN is Zhuhai Seesheen Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for SEESHEEN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970680130073.
What classification code is assigned to this device?
This device is registered under product classification code Z12021006.
Similar Classification Devices (Z12021006)
Other Devices by Zhuhai Seesheen Medical Technology Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint