eudamed_udi
Primary ID: 06979969953792
Analog (UDI 06979969953792)
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 Analog - Primary ID 06979969953792
Device Regulatory Overview
The Analog (Model/Catalog Number: ANL2001(BG)) is a medical device manufactured by Tianjin Coral Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification P01020180 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ANL2001(BG)
- Product Code / EMDN
- P01020180
- Device Name
- Analog
- Database Sync Date
- 2026-08-09 16:28:55
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 Analog?
The registered manufacturer of record for Analog is Tianjin Coral Biotechnology Co., Ltd.
What is the Primary UDI-DI identifier for Analog?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06979969953792.
What classification code is assigned to this device?
This device is registered under product classification code P01020180.
Similar Classification Devices (P01020180)
Other Devices by Tianjin Coral Biotechnology Co., Ltd
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