eudamed_udi
Primary ID: 18052400181475
Quark PFT1 (UDI 18052400181475)
Manufactured by COSMED Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Quark PFT1 - Primary ID 18052400181475
Device Regulatory Overview
The Quark PFT1 (Model/Catalog Number: C09071-11-99) is a medical device manufactured by COSMED Srl. This product is indexed under FDA Product Code / Category Classification Z12150101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C09071-11-99
- Product Code / EMDN
- Z12150101
- Device Name
- Quark SPIRO
- Database Sync Date
- 2026-08-09 17:01:53
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 Quark PFT1?
The registered manufacturer of record for Quark PFT1 is COSMED Srl.
What is the Primary UDI-DI identifier for Quark PFT1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18052400181475.
What classification code is assigned to this device?
This device is registered under product classification code Z12150101.
Similar Classification Devices (Z12150101)
Other Devices by COSMED Srl
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint