gudid
Primary ID: SG-03
Kegel (UDI SG-03)
Manufactured by Star Port Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kegel - Primary ID SG-03
Device Regulatory Overview
The Kegel (Model/Catalog Number: SG-03) is a medical device manufactured by Star Port Inc. This product is indexed under FDA Product Code / Category Classification PFP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SG-03
- Product Code / EMDN
- PFP
- Device Name
- Database Sync Date
- 2026-08-09 09:49:15
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 Kegel?
The registered manufacturer of record for Kegel is Star Port Inc.
What is the Primary UDI-DI identifier for Kegel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SG-03.
What classification code is assigned to this device?
This device is registered under product classification code PFP.
Similar Classification Devices (PFP)
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