Espátula Ayre de madera (UDI 06973697819276)
Manufactured by Jiangsu HanHeng Medical Technology Co., Ltd.
Device Regulatory Overview
The Espátula Ayre de madera (Model/Catalog Number: 11010300) is a medical device manufactured by Jiangsu HanHeng Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification U089002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11010300
- Product Code / EMDN
- U089002
- Device Name
- Disposable Cervical Samplers (non-sterile)
- Database Sync Date
- 2026-08-09 16:29:01
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Espátula Ayre de madera?
The registered manufacturer of record for Espátula Ayre de madera is Jiangsu HanHeng Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for Espátula Ayre de madera?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973697819276.
What classification code is assigned to this device?
This device is registered under product classification code U089002.
Similar Classification Devices (U089002)
Other Devices by Jiangsu HanHeng Medical Technology Co., Ltd.
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