gudid
Primary ID: HS134-MU
SutUp (UDI HS134-MU)
Manufactured by RIVERPOINT MEDICAL, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SutUp - Primary ID HS134-MU
Device Regulatory Overview
The SutUp (Model/Catalog Number: HS134-MU) is a medical device manufactured by RIVERPOINT MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification GAT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HS134-MU
- Product Code / EMDN
- GAT
- Device Name
- Suture
- Database Sync Date
- 2026-08-09 09:12:05
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 SutUp?
The registered manufacturer of record for SutUp is RIVERPOINT MEDICAL, LLC.
What is the Primary UDI-DI identifier for SutUp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HS134-MU.
What classification code is assigned to this device?
This device is registered under product classification code GAT.
Similar Classification Devices (GAT)
Other Devices by RIVERPOINT MEDICAL, LLC
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