eudamed_udi
Primary ID: 06975070996246
Obturator (UDI 06975070996246)
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 Obturator - Primary ID 06975070996246
Device Regulatory Overview
The Obturator (Model/Catalog Number: SP1502) is a medical device manufactured by Shenzhen Edge Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L1399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SP1502
- Product Code / EMDN
- L1399
- Device Name
- Obturator
- Database Sync Date
- 2026-08-09 17:07:24
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 Obturator?
The registered manufacturer of record for Obturator is Shenzhen Edge Medical Co., Ltd..
What is the Primary UDI-DI identifier for Obturator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975070996246.
What classification code is assigned to this device?
This device is registered under product classification code L1399.
Similar Classification Devices (L1399)
Other Devices by Shenzhen Edge Medical Co., Ltd.
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