ROMSONS PERCUTANEOUS TRACHEOSTOMY KIT, ROMO-SOFT CUFF-WDF (UDI 08907265210361)
Manufactured by Romsons Group Private Limited
Device Regulatory Overview
The ROMSONS PERCUTANEOUS TRACHEOSTOMY KIT, ROMO-SOFT CUFF-WDF (Model/Catalog Number: GS-2103W) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification R0105020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS-2103W
- Product Code / EMDN
- R0105020101
- Device Name
- TRACHEOSTOMY TUBE
- Database Sync Date
- 2026-08-09 16:30:13
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 ROMSONS PERCUTANEOUS TRACHEOSTOMY KIT, ROMO-SOFT CUFF-WDF?
The registered manufacturer of record for ROMSONS PERCUTANEOUS TRACHEOSTOMY KIT, ROMO-SOFT CUFF-WDF is Romsons Group Private Limited.
What is the Primary UDI-DI identifier for ROMSONS PERCUTANEOUS TRACHEOSTOMY KIT, ROMO-SOFT CUFF-WDF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265210361.
What classification code is assigned to this device?
This device is registered under product classification code R0105020101.
Similar Classification Devices (R0105020101)
Other Devices by Romsons Group Private Limited
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