eudamed_udi
Primary ID: +G399CTPCP230E
Periodontal Probe (UDI +G399CTPCP230E)
Manufactured by CROSSTEX (PRIVATE) LIMITED.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Periodontal Probe - Primary ID +G399CTPCP230E
Device Regulatory Overview
The Periodontal Probe (Model/Catalog Number: CT-PCP23) is a medical device manufactured by CROSSTEX (PRIVATE) LIMITED.. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CT-PCP23
- Product Code / EMDN
- L159003
- Device Name
- Periodontal Probe
- Database Sync Date
- 2026-08-09 17:01:30
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Periodontal Probe?
The registered manufacturer of record for Periodontal Probe is CROSSTEX (PRIVATE) LIMITED..
What is the Primary UDI-DI identifier for Periodontal Probe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G399CTPCP230E.
What classification code is assigned to this device?
This device is registered under product classification code L159003.
Similar Classification Devices (L159003)
Other Devices by CROSSTEX (PRIVATE) LIMITED.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint