Vereos PET/CT System Upgrade (UDI 00884838108103)
Manufactured by Philips Medical Systems Nederland B.V.
Device Regulatory Overview
The Vereos PET/CT System Upgrade (Model/Catalog Number: 882425) is a medical device manufactured by Philips Medical Systems Nederland B.V.. This product is indexed under FDA Product Code / Category Classification Z11020301 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
- 882425
- Product Code / EMDN
- Z11020301
- Device Name
- Vereos PET/CT System
- Database Sync Date
- 2026-08-09 16:50:32
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 Vereos PET/CT System Upgrade?
The registered manufacturer of record for Vereos PET/CT System Upgrade is Philips Medical Systems Nederland B.V..
What is the Primary UDI-DI identifier for Vereos PET/CT System Upgrade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838108103.
What classification code is assigned to this device?
This device is registered under product classification code Z11020301.
Similar Classification Devices (Z11020301)
Other Devices by Philips Medical Systems Nederland B.V.
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