Sterile Wound Plasters (UDI 06925923785183)
Manufactured by Hynaut Health Technology Co., LTD
Device Regulatory Overview
The Sterile Wound Plasters (Model/Catalog Number: C101-C119) is a medical device manufactured by Hynaut Health Technology Co., LTD. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C101-C119
- Product Code / EMDN
- M04010101
- Device Name
- Sterile Wound Plasters
- Database Sync Date
- 2026-08-09 16:30:04
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 Sterile Wound Plasters?
The registered manufacturer of record for Sterile Wound Plasters is Hynaut Health Technology Co., LTD.
What is the Primary UDI-DI identifier for Sterile Wound Plasters?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925923785183.
What classification code is assigned to this device?
This device is registered under product classification code M04010101.
Similar Classification Devices (M04010101)
Other Devices by Hynaut Health Technology Co., LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint