gudid
Primary ID: J2700
CamX Triton HD, Cam Spectra Proxi (UDI J2700)
Manufactured by DRR DENTAL SE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CamX Triton HD, Cam Spectra Proxi - Primary ID J2700
Device Regulatory Overview
The CamX Triton HD, Cam Spectra Proxi (Model/Catalog Number: J2700) is a medical device manufactured by DRR DENTAL SE. This product is indexed under FDA Product Code / Category Classification NTK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- J2700
- Product Code / EMDN
- NTK
- Device Name
- Database Sync Date
- 2026-08-09 09:07:32
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 CamX Triton HD, Cam Spectra Proxi?
The registered manufacturer of record for CamX Triton HD, Cam Spectra Proxi is DRR DENTAL SE.
What is the Primary UDI-DI identifier for CamX Triton HD, Cam Spectra Proxi?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J2700.
What classification code is assigned to this device?
This device is registered under product classification code NTK.
Similar Classification Devices (NTK)
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