GUDIDData
eudamed_udi Primary ID: 06973122514059

KIT LITERIE NON STERILE USAGE UNIQUE (UDI 06973122514059)

Manufactured by Crown Name Disposable Hygiene Products Fty. Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIT LITERIE NON STERILE USAGE UNIQUE - Primary ID 06973122514059

Device Regulatory Overview

The KIT LITERIE NON STERILE USAGE UNIQUE (Model/Catalog Number: BK-1L) is a medical device manufactured by Crown Name Disposable Hygiene Products Fty. Ltd.. This product is indexed under FDA Product Code / Category Classification T030599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BK-1L
Product Code / EMDN
T030599
Device Name
Bedding
Database Sync Date
2026-08-09 16:45:07

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 KIT LITERIE NON STERILE USAGE UNIQUE?

The registered manufacturer of record for KIT LITERIE NON STERILE USAGE UNIQUE is Crown Name Disposable Hygiene Products Fty. Ltd..

What is the Primary UDI-DI identifier for KIT LITERIE NON STERILE USAGE UNIQUE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973122514059.

What classification code is assigned to this device?

This device is registered under product classification code T030599.

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