Arcovis DRF (UDI 08055186671119)
Manufactured by A.T.S. Applicazione Tecnologie Speciali s.r.l.
Device Regulatory Overview
The Arcovis DRF (Model/Catalog Number: 74 09 000-2; 74 11 000-2) is a medical device manufactured by A.T.S. Applicazione Tecnologie Speciali s.r.l.. This product is indexed under FDA Product Code / Category Classification Z11039017 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 74 09 000-2; 74 11 000-2
- Product Code / EMDN
- Z11039017
- Device Name
- ARCO FP
- Database Sync Date
- 2026-08-09 16:48:02
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 Arcovis DRF?
The registered manufacturer of record for Arcovis DRF is A.T.S. Applicazione Tecnologie Speciali s.r.l..
What is the Primary UDI-DI identifier for Arcovis DRF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055186671119.
What classification code is assigned to this device?
This device is registered under product classification code Z11039017.
Similar Classification Devices (Z11039017)
Other Devices by A.T.S. Applicazione Tecnologie Speciali s.r.l.
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