gudid
Primary ID: C200030
RINN (UDI C200030)
Manufactured by Dentsply International Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RINN - Primary ID C200030
Device Regulatory Overview
The RINN (Model/Catalog Number: C200030) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EHK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C200030
- Product Code / EMDN
- EHK
- Device Name
- Crescent Prophy Cups RA Webbed
- Database Sync Date
- 2026-08-09 09:02:02
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 RINN?
The registered manufacturer of record for RINN is Dentsply International Inc..
What is the Primary UDI-DI identifier for RINN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C200030.
What classification code is assigned to this device?
This device is registered under product classification code EHK.
Similar Classification Devices (EHK)
Other Devices by Dentsply International Inc.
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