eudamed_udi
Primary ID: 06975070992637
Cannula (UDI 06975070992637)
Manufactured by Shenzhen Edge Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cannula - Primary ID 06975070992637
Device Regulatory Overview
The Cannula (Model/Catalog Number: TR1-A8I) is a medical device manufactured by Shenzhen Edge Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L1207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TR1-A8I
- Product Code / EMDN
- L1207
- Device Name
- Cannula
- Database Sync Date
- 2026-08-09 16:44:49
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 Cannula?
The registered manufacturer of record for Cannula is Shenzhen Edge Medical Co., Ltd..
What is the Primary UDI-DI identifier for Cannula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975070992637.
What classification code is assigned to this device?
This device is registered under product classification code L1207.
Similar Classification Devices (L1207)
Other Devices by Shenzhen Edge Medical Co., Ltd.
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