eudamed_udi
Primary ID: 00606959042551
Philips Basic Kit, PerformaTrak SE, INTL (UDI 00606959042551)
Manufactured by Respironics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Philips Basic Kit, PerformaTrak SE, INTL - Primary ID 00606959042551
Device Regulatory Overview
The Philips Basic Kit, PerformaTrak SE, INTL (Model/Catalog Number: 1074050) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification Z12062402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1074050
- Product Code / EMDN
- Z12062402
- Device Name
- PerformaTrak SE Disposable Full Face Mask
- Database Sync Date
- 2026-08-09 19:08:05
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 Philips Basic Kit, PerformaTrak SE, INTL?
The registered manufacturer of record for Philips Basic Kit, PerformaTrak SE, INTL is Respironics Inc..
What is the Primary UDI-DI identifier for Philips Basic Kit, PerformaTrak SE, INTL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959042551.
What classification code is assigned to this device?
This device is registered under product classification code Z12062402.
Similar Classification Devices (Z12062402)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint