GUDIDData
gudid Primary ID: JB0112-071

JOHN BUNN (UDI JB0112-071)

Manufactured by GF HEALTH PRODUCTS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JOHN BUNN - Primary ID JB0112-071

Device Regulatory Overview

The JOHN BUNN (Model/Catalog Number: JB0112-071) is a medical device manufactured by GF HEALTH PRODUCTS, INC.. This product is indexed under FDA Product Code / Category Classification BTI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
JB0112-071
Product Code / EMDN
BTI
Device Name
Neb-u-Tyke Nebulizer Compressor
Database Sync Date
2026-08-09 09:14:40

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 JOHN BUNN?

The registered manufacturer of record for JOHN BUNN is GF HEALTH PRODUCTS, INC..

What is the Primary UDI-DI identifier for JOHN BUNN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is JB0112-071.

What classification code is assigned to this device?

This device is registered under product classification code BTI.

Programmatic Export

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

JSON API Endpoint