Ruschelit Safety ClearTracheal Tube, Oral/Nasal (UDI 14026704332912)
Manufactured by Teleflex Medical Sdn. Bhd.
Device Regulatory Overview
The Ruschelit Safety ClearTracheal Tube, Oral/Nasal (Model/Catalog Number: 100380-000080) is a medical device manufactured by Teleflex Medical Sdn. Bhd.. This product is indexed under FDA Product Code / Category Classification R01030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100380-000080
- Product Code / EMDN
- R01030101
- Device Name
- TRACHEAL TUBE
- Database Sync Date
- 2026-08-09 16:46:28
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 Ruschelit Safety ClearTracheal Tube, Oral/Nasal?
The registered manufacturer of record for Ruschelit Safety ClearTracheal Tube, Oral/Nasal is Teleflex Medical Sdn. Bhd..
What is the Primary UDI-DI identifier for Ruschelit Safety ClearTracheal Tube, Oral/Nasal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14026704332912.
What classification code is assigned to this device?
This device is registered under product classification code R01030101.
Similar Classification Devices (R01030101)
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