CITOTEST (UDI 06942826217368)
Manufactured by CITOTEST LABWARE MANUFACTURING CO.,LTD
Device Regulatory Overview
The CITOTEST (Model/Catalog Number: 4320-1701) is a medical device manufactured by CITOTEST LABWARE MANUFACTURING CO.,LTD. This product is indexed under FDA Product Code / Category Classification W0503020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4320-1701
- Product Code / EMDN
- W0503020199
- Device Name
- Pasteur Pipette
- Database Sync Date
- 2026-08-09 16:29:03
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 CITOTEST?
The registered manufacturer of record for CITOTEST is CITOTEST LABWARE MANUFACTURING CO.,LTD.
What is the Primary UDI-DI identifier for CITOTEST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942826217368.
What classification code is assigned to this device?
This device is registered under product classification code W0503020199.
Similar Classification Devices (W0503020199)
Other Devices by CITOTEST LABWARE MANUFACTURING CO.,LTD
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