eudamed_udi
Primary ID: 06979969951101
Screw (UDI 06979969951101)
Manufactured by Tianjin Coral Biotechnology Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Screw - Primary ID 06979969951101
Device Regulatory Overview
The Screw (Model/Catalog Number: SCW1901(IX)) is a medical device manufactured by Tianjin Coral Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification Q010280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SCW1901(IX)
- Product Code / EMDN
- Q010280
- Device Name
- Screw
- Database Sync Date
- 2026-08-09 16:28:56
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 Screw?
The registered manufacturer of record for Screw is Tianjin Coral Biotechnology Co., Ltd.
What is the Primary UDI-DI identifier for Screw?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06979969951101.
What classification code is assigned to this device?
This device is registered under product classification code Q010280.
Similar Classification Devices (Q010280)
Other Devices by Tianjin Coral Biotechnology Co., Ltd
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