GUDIDData
gudid Primary ID: 2742.1101-O

VOLMED BRASIL (UDI 2742.1101-O)

Manufactured by VOLMED BRASIL EQUIPAMENTOS LTDA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VOLMED BRASIL - Primary ID 2742.1101-O

Device Regulatory Overview

The VOLMED BRASIL (Model/Catalog Number: 2742.1101-O) is a medical device manufactured by VOLMED BRASIL EQUIPAMENTOS LTDA. This product is indexed under FDA Product Code / Category Classification NBH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2742.1101-O
Product Code / EMDN
NBH
Device Name
MINI CANNULA FOR AGGRESSIVE INCISOR MICRODEBIDEMENT 4,5-115-Straight-RZM
Database Sync Date
2026-08-09 09:05:13

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 VOLMED BRASIL?

The registered manufacturer of record for VOLMED BRASIL is VOLMED BRASIL EQUIPAMENTOS LTDA.

What is the Primary UDI-DI identifier for VOLMED BRASIL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2742.1101-O.

What classification code is assigned to this device?

This device is registered under product classification code NBH.

Programmatic Export

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

JSON API Endpoint