eudamed_udi
Primary ID: 00884838120136
FloTrac (UDI 00884838120136)
Manufactured by Philips Medizin Systeme Böblingen GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FloTrac - Primary ID 00884838120136
Device Regulatory Overview
The FloTrac (Model/Catalog Number: 867409) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z12030280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 867409
- Product Code / EMDN
- Z12030280
- Device Name
- Hemodynamic Monitoring Module
- Database Sync Date
- 2026-08-09 16:48:04
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of FloTrac?
The registered manufacturer of record for FloTrac is Philips Medizin Systeme Böblingen GmbH.
What is the Primary UDI-DI identifier for FloTrac?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838120136.
What classification code is assigned to this device?
This device is registered under product classification code Z12030280.
Similar Classification Devices (Z12030280)
Other Devices by Philips Medizin Systeme Böblingen GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint