gudid
Primary ID: P200-CA-4
Primado2 (UDI P200-CA-4)
Manufactured by NAKANISHI INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Primado2 - Primary ID P200-CA-4
Device Regulatory Overview
The Primado2 (Model/Catalog Number: P200-CA-4) is a medical device manufactured by NAKANISHI INC.. This product is indexed under FDA Product Code / Category Classification HBC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P200-CA-4
- Product Code / EMDN
- HBC
- Device Name
- Database Sync Date
- 2026-08-09 09:15:39
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 Primado2?
The registered manufacturer of record for Primado2 is NAKANISHI INC..
What is the Primary UDI-DI identifier for Primado2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P200-CA-4.
What classification code is assigned to this device?
This device is registered under product classification code HBC.
Similar Classification Devices (HBC)
Other Devices by NAKANISHI INC.
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