eudamed_udi
Primary ID: 07613365003536
CARDIOVIT FT-2 (UDI 07613365003536)
Manufactured by SCHILLER AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CARDIOVIT FT-2 - Primary ID 07613365003536
Device Regulatory Overview
The CARDIOVIT FT-2 (Model/Catalog Number: 3.900880) is a medical device manufactured by SCHILLER AG. This product is indexed under FDA Product Code / Category Classification Z12050301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3.900880
- Product Code / EMDN
- Z12050301
- Device Name
- CARDIOVIT FT-2
- Database Sync Date
- 2026-08-09 18:06:04
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 CARDIOVIT FT-2?
The registered manufacturer of record for CARDIOVIT FT-2 is SCHILLER AG.
What is the Primary UDI-DI identifier for CARDIOVIT FT-2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613365003536.
What classification code is assigned to this device?
This device is registered under product classification code Z12050301.
Similar Classification Devices (Z12050301)
Other Devices by SCHILLER AG
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