Cheek retractor (UDI 06978049070091)
Manufactured by Anson Investment Development Co.,Ltd.
Device Regulatory Overview
The Cheek retractor (Model/Catalog Number: KOQ01S) is a medical device manufactured by Anson Investment Development Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification L150201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KOQ01S
- Product Code / EMDN
- L150201
- Device Name
- cheek retractor
- Database Sync Date
- 2026-08-09 16:29:20
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 Cheek retractor?
The registered manufacturer of record for Cheek retractor is Anson Investment Development Co.,Ltd..
What is the Primary UDI-DI identifier for Cheek retractor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978049070091.
What classification code is assigned to this device?
This device is registered under product classification code L150201.
Similar Classification Devices (L150201)
Other Devices by Anson Investment Development Co.,Ltd.
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