GUDIDData
eudamed_udi Primary ID: +G399CTCVM10D

Carvers (UDI +G399CTCVM10D)

Manufactured by CROSSTEX (PRIVATE) LIMITED.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Carvers - Primary ID +G399CTCVM10D

Device Regulatory Overview

The Carvers (Model/Catalog Number: CT-CVM1) is a medical device manufactured by CROSSTEX (PRIVATE) LIMITED.. This product is indexed under FDA Product Code / Category Classification L159017 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CT-CVM1
Product Code / EMDN
L159017
Device Name
Carvers
Database Sync Date
2026-08-09 16:46:34

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 Carvers?

The registered manufacturer of record for Carvers is CROSSTEX (PRIVATE) LIMITED..

What is the Primary UDI-DI identifier for Carvers?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G399CTCVM10D.

What classification code is assigned to this device?

This device is registered under product classification code L159017.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint