Gauze Pad (UDI 06925923795465)
Manufactured by Hynaut Health Technology Co., LTD
Device Regulatory Overview
The Gauze Pad (Model/Catalog Number: C170\C171\C172\C173\C174\C175\C176\C177\C178\C179) is a medical device manufactured by Hynaut Health Technology Co., LTD. This product is indexed under FDA Product Code / Category Classification M0201020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C170\C171\C172\C173\C174\C175\C176\C177\C178\C179
- Product Code / EMDN
- M0201020101
- Device Name
- Surgical Sponges
- Database Sync Date
- 2026-08-09 18:51:44
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 Gauze Pad?
The registered manufacturer of record for Gauze Pad is Hynaut Health Technology Co., LTD.
What is the Primary UDI-DI identifier for Gauze Pad?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925923795465.
What classification code is assigned to this device?
This device is registered under product classification code M0201020101.
Similar Classification Devices (M0201020101)
Other Devices by Hynaut Health Technology Co., LTD
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