eudamed_udi
Primary ID: 05021300770740
K-Lite 7cm x 4.5M (UDI 05021300770740)
Manufactured by urgo ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for K-Lite 7cm x 4.5M - Primary ID 05021300770740
Device Regulatory Overview
The K-Lite 7cm x 4.5M (Model/Catalog Number: 190482) is a medical device manufactured by urgo ltd. This product is indexed under FDA Product Code / Category Classification M0304010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 190482
- Product Code / EMDN
- M0304010102
- Device Name
- K-Lite
- Database Sync Date
- 2026-08-09 16:46:28
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of K-Lite 7cm x 4.5M?
The registered manufacturer of record for K-Lite 7cm x 4.5M is urgo ltd.
What is the Primary UDI-DI identifier for K-Lite 7cm x 4.5M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05021300770740.
What classification code is assigned to this device?
This device is registered under product classification code M0304010102.
Similar Classification Devices (M0304010102)
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