eudamed_udi
Primary ID: 07350040975930
Remote Review Software Version Independent (UDI 07350040975930)
Manufactured by CellaVision AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Remote Review Software Version Independent - Primary ID 07350040975930
Device Regulatory Overview
The Remote Review Software Version Independent (Model/Catalog Number: AG516335) 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
- AG516335
- Product Code / EMDN
- W02029092
- Device Name
- CellaVision® Review Software
- Database Sync Date
- 2026-08-09 16:28:59
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 Remote Review Software Version Independent?
The registered manufacturer of record for Remote Review Software Version Independent is CellaVision AB.
What is the Primary UDI-DI identifier for Remote Review Software Version Independent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350040975930.
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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