CARESCAPE Canvas D19 (UDI 5897061)
Manufactured by GE Healthcare Finland Oy
Device Regulatory Overview
The CARESCAPE Canvas D19 (Model/Catalog Number: 5897061) is a medical device manufactured by GE Healthcare Finland Oy. This product is indexed under FDA Product Code / Category Classification CBS within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 5897061
- Product Code / EMDN
- CBS
- Device Name
- CARESCAPE Canvas D19
- Database Sync Date
- 2026-08-09 09:14:30
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 CARESCAPE Canvas D19?
The registered manufacturer of record for CARESCAPE Canvas D19 is GE Healthcare Finland Oy.
What is the Primary UDI-DI identifier for CARESCAPE Canvas D19?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5897061.
What classification code is assigned to this device?
This device is registered under product classification code CBS.
Similar Classification Devices (CBS)
Other Devices by GE Healthcare Finland Oy
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