GUDIDData
eudamed_udi Primary ID: 00606959021389

CoughAssist E70 Series Oximetry Interface Kit (UDI 00606959021389)

Manufactured by Respironics Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CoughAssist E70 Series Oximetry Interface Kit - Primary ID 00606959021389

Device Regulatory Overview

The CoughAssist E70 Series Oximetry Interface Kit (Model/Catalog Number: 1098718) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1098718
Product Code / EMDN
R05010301
Device Name
CoughAssist E70 Series Oximetry Interface Kit
Database Sync Date
2026-08-09 16:29:04

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 CoughAssist E70 Series Oximetry Interface Kit?

The registered manufacturer of record for CoughAssist E70 Series Oximetry Interface Kit is Respironics Inc..

What is the Primary UDI-DI identifier for CoughAssist E70 Series Oximetry Interface Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959021389.

What classification code is assigned to this device?

This device is registered under product classification code R05010301.

Programmatic Export

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

JSON API Endpoint