GUDIDData
eudamed_udi Primary ID: 00606959021365

CoughAssist 70 Series Circuit, Adult Large, 9ft (UDI 00606959021365)

Manufactured by Respironics Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CoughAssist 70 Series Circuit, Adult Large, 9ft - Primary ID 00606959021365

Device Regulatory Overview

The CoughAssist 70 Series Circuit, Adult Large, 9ft (Model/Catalog Number: 1098408) 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
1098408
Product Code / EMDN
R05010301
Device Name
CoughAssist Class IIa Accessories
Database Sync Date
2026-08-09 16:58:28

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of CoughAssist 70 Series Circuit, Adult Large, 9ft?

The registered manufacturer of record for CoughAssist 70 Series Circuit, Adult Large, 9ft is Respironics Inc..

What is the Primary UDI-DI identifier for CoughAssist 70 Series Circuit, Adult Large, 9ft?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959021365.

What classification code is assigned to this device?

This device is registered under product classification code R05010301.

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