Dental Root-Canal Instruments (UDI 06941422600277)
Manufactured by Shenzhen Perfect Medical Instruments Co., Ltd.
Device Regulatory Overview
The Dental Root-Canal Instruments (Model/Catalog Number: SSS,#A) is a medical device manufactured by Shenzhen Perfect Medical Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Q010507 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SSS,#A
- Product Code / EMDN
- Q010507
- Device Name
- Dental Root-Canal Instruments
- Database Sync Date
- 2026-08-09 16:28:45
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 Dental Root-Canal Instruments?
The registered manufacturer of record for Dental Root-Canal Instruments is Shenzhen Perfect Medical Instruments Co., Ltd..
What is the Primary UDI-DI identifier for Dental Root-Canal Instruments?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06941422600277.
What classification code is assigned to this device?
This device is registered under product classification code Q010507.
Similar Classification Devices (Q010507)
Other Devices by Shenzhen Perfect Medical Instruments Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint