CellaVision® Adv. RBC and Body Fluid DM9600 Non-Expiring License (UDI 07350040974940)
Manufactured by CellaVision AB
Device Regulatory Overview
The CellaVision® Adv. RBC and Body Fluid DM9600 Non-Expiring License (Model/Catalog Number: CAB-970099) is a medical device manufactured by CellaVision AB. This product is indexed under FDA Product Code / Category Classification W02029092 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CAB-970099
- Product Code / EMDN
- W02029092
- Device Name
- CellaVision® Adv. RBC and Body Fluid
- Database Sync Date
- 2026-08-09 18:48:59
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 CellaVision® Adv. RBC and Body Fluid DM9600 Non-Expiring License?
The registered manufacturer of record for CellaVision® Adv. RBC and Body Fluid DM9600 Non-Expiring License is CellaVision AB.
What is the Primary UDI-DI identifier for CellaVision® Adv. RBC and Body Fluid DM9600 Non-Expiring License?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350040974940.
What classification code is assigned to this device?
This device is registered under product classification code W02029092.
Similar Classification Devices (W02029092)
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