eudamed_udi
Primary ID: 00850015358449
Rigicon (UDI 00850015358449)
Manufactured by Rigicon, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rigicon - Primary ID 00850015358449
Device Regulatory Overview
The Rigicon (Model/Catalog Number: RSUD-1012) is a medical device manufactured by Rigicon, Inc.. This product is indexed under FDA Product Code / Category Classification K01020117 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RSUD-1012
- Product Code / EMDN
- K01020117
- Device Name
- Rigicon HL Dilator (Sterile)
- Database Sync Date
- 2026-08-09 17:09:17
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 Rigicon?
The registered manufacturer of record for Rigicon is Rigicon, Inc..
What is the Primary UDI-DI identifier for Rigicon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850015358449.
What classification code is assigned to this device?
This device is registered under product classification code K01020117.
Similar Classification Devices (K01020117)
Other Devices by Rigicon, Inc.
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