gudid
Primary ID: FC-83
FC-83 (UDI FC-83)
Manufactured by NAKANISHI INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FC-83 - Primary ID FC-83
Device Regulatory Overview
The FC-83 (Model/Catalog Number: FC-83) is a medical device manufactured by NAKANISHI INC.. This product is indexed under FDA Product Code / Category Classification KOJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FC-83
- Product Code / EMDN
- KOJ
- Device Name
- Database Sync Date
- 2026-08-09 09:15:32
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 FC-83?
The registered manufacturer of record for FC-83 is NAKANISHI INC..
What is the Primary UDI-DI identifier for FC-83?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FC-83.
What classification code is assigned to this device?
This device is registered under product classification code KOJ.
Similar Classification Devices (KOJ)
Other Devices by NAKANISHI INC.
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