eudamed_udi
Primary ID: 04260502643457
PROSLIDE 32 SR System (UDI 04260502643457)
Manufactured by PROTEC X-ray Systems GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROSLIDE 32 SR System - Primary ID 04260502643457
Device Regulatory Overview
The PROSLIDE 32 SR System (Model/Catalog Number: 7016-9-0000_V007) is a medical device manufactured by PROTEC X-ray Systems GmbH. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7016-9-0000_V007
- Product Code / EMDN
- Z11039016
- Device Name
- PROSLIDE 32 SR System
- Database Sync Date
- 2026-08-09 16:46:22
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 PROSLIDE 32 SR System?
The registered manufacturer of record for PROSLIDE 32 SR System is PROTEC X-ray Systems GmbH.
What is the Primary UDI-DI identifier for PROSLIDE 32 SR System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260502643457.
What classification code is assigned to this device?
This device is registered under product classification code Z11039016.
Similar Classification Devices (Z11039016)
Other Devices by PROTEC X-ray Systems GmbH
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