Dual Cytocuvette - medium absorption (UDI 08033976237189)
Manufactured by Bio-Optica Milano S.p.A.
Device Regulatory Overview
The Dual Cytocuvette - medium absorption (Model/Catalog Number: 14-080) is a medical device manufactured by Bio-Optica Milano S.p.A.. This product is indexed under FDA Product Code / Category Classification W0503010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 14-080
- Product Code / EMDN
- W0503010203
- Device Name
- Dual Cytocuvette
- Database Sync Date
- 2026-08-09 19:04:33
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 Dual Cytocuvette - medium absorption?
The registered manufacturer of record for Dual Cytocuvette - medium absorption is Bio-Optica Milano S.p.A..
What is the Primary UDI-DI identifier for Dual Cytocuvette - medium absorption?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033976237189.
What classification code is assigned to this device?
This device is registered under product classification code W0503010203.
Similar Classification Devices (W0503010203)
Other Devices by Bio-Optica Milano S.p.A.
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