GUDIDData
eudamed_udi Primary ID: 15060069282863

Cath It Removal Pack Medium (UDI 15060069282863)

Manufactured by Richardson Healthcare Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cath It Removal Pack Medium - Primary ID 15060069282863

Device Regulatory Overview

The Cath It Removal Pack Medium (Model/Catalog Number: 908422) is a medical device manufactured by Richardson Healthcare Limited. This product is indexed under FDA Product Code / Category Classification T0203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
908422
Product Code / EMDN
T0203
Device Name
Cath It Removal Pack Medium
Database Sync Date
2026-08-09 16:48:20

Full Regulatory Attributes

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{
    "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 Cath It Removal Pack Medium?

The registered manufacturer of record for Cath It Removal Pack Medium is Richardson Healthcare Limited.

What is the Primary UDI-DI identifier for Cath It Removal Pack Medium?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15060069282863.

What classification code is assigned to this device?

This device is registered under product classification code T0203.

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