ENDOTRACHEAL TUBE CUFFED (UDI 08907265010497)
Manufactured by Romsons Group Private Limited
Device Regulatory Overview
The ENDOTRACHEAL TUBE CUFFED (Model/Catalog Number: GS-2004 KAD) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification R01030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS-2004 KAD
- Product Code / EMDN
- R01030201
- Device Name
- ENDOTRACHEAL TUBE
- Database Sync Date
- 2026-08-09 16:29:13
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 ENDOTRACHEAL TUBE CUFFED?
The registered manufacturer of record for ENDOTRACHEAL TUBE CUFFED is Romsons Group Private Limited.
What is the Primary UDI-DI identifier for ENDOTRACHEAL TUBE CUFFED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265010497.
What classification code is assigned to this device?
This device is registered under product classification code R01030201.
Similar Classification Devices (R01030201)
Other Devices by Romsons Group Private Limited
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