GUDIDData
gudid Primary ID: IPN049948

RUSCH (UDI IPN049948)

Manufactured by TELEFLEX INCORPORATED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RUSCH - Primary ID IPN049948

Device Regulatory Overview

The RUSCH (Model/Catalog Number: IPN049948) is a medical device manufactured by TELEFLEX INCORPORATED. This product is indexed under FDA Product Code / Category Classification CCW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
IPN049948
Product Code / EMDN
CCW
Device Name
Emerald Fiber Optic Laryngoscope Blade Miller Size 3
Database Sync Date
2026-08-09 09:00:28

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 RUSCH?

The registered manufacturer of record for RUSCH is TELEFLEX INCORPORATED.

What is the Primary UDI-DI identifier for RUSCH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IPN049948.

What classification code is assigned to this device?

This device is registered under product classification code CCW.

Programmatic Export

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

JSON API Endpoint