eudamed_udi
Primary ID: 18052400180461
K5 (UDI 18052400180461)
Manufactured by COSMED Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for K5 - Primary ID 18052400180461
Device Regulatory Overview
The K5 (Model/Catalog Number: C09090-01-99) is a medical device manufactured by COSMED Srl. This product is indexed under FDA Product Code / Category Classification Z12050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C09090-01-99
- Product Code / EMDN
- Z12050101
- Device Name
- K5
- Database Sync Date
- 2026-08-09 18:50:51
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 K5?
The registered manufacturer of record for K5 is COSMED Srl.
What is the Primary UDI-DI identifier for K5?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18052400180461.
What classification code is assigned to this device?
This device is registered under product classification code Z12050101.
Similar Classification Devices (Z12050101)
Other Devices by COSMED Srl
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