CYTO CUVETTE KIT 2 - 2 pozzetti, vetrino serigrafato a 2 cerchi (UDI 08055510562892)
Manufactured by Kaltek S.r.l.
Device Regulatory Overview
The CYTO CUVETTE KIT 2 - 2 pozzetti, vetrino serigrafato a 2 cerchi (Model/Catalog Number: 0773) is a medical device manufactured by Kaltek S.r.l.. This product is indexed under FDA Product Code / Category Classification W0503010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0773
- Product Code / EMDN
- W0503010203
- Device Name
- CUVETTE
- Database Sync Date
- 2026-08-09 17:08:46
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 CYTO CUVETTE KIT 2 - 2 pozzetti, vetrino serigrafato a 2 cerchi?
The registered manufacturer of record for CYTO CUVETTE KIT 2 - 2 pozzetti, vetrino serigrafato a 2 cerchi is Kaltek S.r.l..
What is the Primary UDI-DI identifier for CYTO CUVETTE KIT 2 - 2 pozzetti, vetrino serigrafato a 2 cerchi?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055510562892.
What classification code is assigned to this device?
This device is registered under product classification code W0503010203.
Similar Classification Devices (W0503010203)
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