eudamed_udi
Primary ID: 06956014455265
SafeCut (UDI 06956014455265)
Manufactured by Shunmei Medical Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SafeCut - Primary ID 06956014455265
Device Regulatory Overview
The SafeCut (Model/Catalog Number: 635526) is a medical device manufactured by Shunmei Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification C010401020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 635526
- Product Code / EMDN
- C010401020101
- Device Name
- Coronary Cutting Balloon Dilatation Catheter
- Database Sync Date
- 2026-08-09 16:28:58
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 SafeCut?
The registered manufacturer of record for SafeCut is Shunmei Medical Co.,Ltd.
What is the Primary UDI-DI identifier for SafeCut?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06956014455265.
What classification code is assigned to this device?
This device is registered under product classification code C010401020101.
Similar Classification Devices (C010401020101)
Other Devices by Shunmei Medical Co.,Ltd
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