ProLine PercuTrach® Cuff Voice, Gr.7 mit atraumatischer Einführhilfe steril, nicht MRT geeignet (UDI 04250203258852)
Manufactured by Primed Halberstadt Medizintechnik GmbH
Device Regulatory Overview
The ProLine PercuTrach® Cuff Voice, Gr.7 mit atraumatischer Einführhilfe steril, nicht MRT geeignet (Model/Catalog Number: 1021570) is a medical device manufactured by Primed Halberstadt Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification R0105020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1021570
- Product Code / EMDN
- R0105020101
- Device Name
- ProLine und Optima PercuTrach Sets
- Database Sync Date
- 2026-08-09 16:47:00
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 ProLine PercuTrach® Cuff Voice, Gr.7 mit atraumatischer Einführhilfe steril, nicht MRT geeignet?
The registered manufacturer of record for ProLine PercuTrach® Cuff Voice, Gr.7 mit atraumatischer Einführhilfe steril, nicht MRT geeignet is Primed Halberstadt Medizintechnik GmbH.
What is the Primary UDI-DI identifier for ProLine PercuTrach® Cuff Voice, Gr.7 mit atraumatischer Einführhilfe steril, nicht MRT geeignet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250203258852.
What classification code is assigned to this device?
This device is registered under product classification code R0105020101.
Similar Classification Devices (R0105020101)
Other Devices by Primed Halberstadt Medizintechnik GmbH
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