PercuTrach® PDT-Set Typ 2 + Optima Basic Cuff, Gr.7ohne Spreizzange, steril (UDI 04250203274340)
Manufactured by Primed Halberstadt Medizintechnik GmbH
Device Regulatory Overview
The PercuTrach® PDT-Set Typ 2 + Optima Basic Cuff, Gr.7ohne Spreizzange, steril (Model/Catalog Number: 112364) 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
- 112364
- Product Code / EMDN
- R0105020101
- Device Name
- ProLine und Optima PDT Sets
- Database Sync Date
- 2026-08-09 16:47:18
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 PercuTrach® PDT-Set Typ 2 + Optima Basic Cuff, Gr.7ohne Spreizzange, steril?
The registered manufacturer of record for PercuTrach® PDT-Set Typ 2 + Optima Basic Cuff, Gr.7ohne Spreizzange, steril is Primed Halberstadt Medizintechnik GmbH.
What is the Primary UDI-DI identifier for PercuTrach® PDT-Set Typ 2 + Optima Basic Cuff, Gr.7ohne Spreizzange, steril?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250203274340.
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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