GUDIDData
eudamed_udi Primary ID: 06948538369166

Respiration Data Management Software (UDI 06948538369166)

Manufactured by BMC Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Respiration Data Management Software - Primary ID 06948538369166

Device Regulatory Overview

The Respiration Data Management Software (Model/Catalog Number: PAP Link(App)) is a medical device manufactured by BMC Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12159092 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PAP Link(App)
Product Code / EMDN
Z12159092
Device Name
Respiration Data Management Software
Database Sync Date
2026-08-09 16:49:00

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 Respiration Data Management Software?

The registered manufacturer of record for Respiration Data Management Software is BMC Medical Co., Ltd..

What is the Primary UDI-DI identifier for Respiration Data Management Software?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06948538369166.

What classification code is assigned to this device?

This device is registered under product classification code Z12159092.

Programmatic Export

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

JSON API Endpoint