eudamed_udi
Primary ID: 06976262792851
BINFEI (UDI 06976262792851)
Manufactured by ZHUCHENG BINFEI MEDI-TEK CO.,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BINFEI - Primary ID 06976262792851
Device Regulatory Overview
The BINFEI (Model/Catalog Number: A00128) is a medical device manufactured by ZHUCHENG BINFEI MEDI-TEK CO.,LTD. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A00128
- Product Code / EMDN
- Q010503
- Device Name
- Dental cheek tray
- Database Sync Date
- 2026-08-09 16:30:07
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 BINFEI?
The registered manufacturer of record for BINFEI is ZHUCHENG BINFEI MEDI-TEK CO.,LTD.
What is the Primary UDI-DI identifier for BINFEI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976262792851.
What classification code is assigned to this device?
This device is registered under product classification code Q010503.
Similar Classification Devices (Q010503)
Other Devices by ZHUCHENG BINFEI MEDI-TEK CO.,LTD
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