eudamed_udi
Primary ID: 06956014403129
Shun Pivot® (UDI 06956014403129)
Manufactured by Shunmei Medical Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Shun Pivot® - Primary ID 06956014403129
Device Regulatory Overview
The Shun Pivot® (Model/Catalog Number: 610312) is a medical device manufactured by Shunmei Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification F900201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 610312
- Product Code / EMDN
- F900201
- Device Name
- Hemodialysis Catheter Kits
- Database Sync Date
- 2026-08-09 16:50:18
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 Shun Pivot®?
The registered manufacturer of record for Shun Pivot® is Shunmei Medical Co.,Ltd.
What is the Primary UDI-DI identifier for Shun Pivot®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06956014403129.
What classification code is assigned to this device?
This device is registered under product classification code F900201.
Similar Classification Devices (F900201)
Other Devices by Shunmei Medical Co.,Ltd
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