eudamed_udi
Primary ID: 08907265000375
NELATON CATHETER (UDI 08907265000375)
Manufactured by Romsons Group Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NELATON CATHETER - Primary ID 08907265000375
Device Regulatory Overview
The NELATON CATHETER (Model/Catalog Number: GS-1004F) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification U01010502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS-1004F
- Product Code / EMDN
- U01010502
- Device Name
- NELATON CATHETER
- Database Sync Date
- 2026-08-09 16:28:44
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 NELATON CATHETER?
The registered manufacturer of record for NELATON CATHETER is Romsons Group Private Limited.
What is the Primary UDI-DI identifier for NELATON CATHETER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265000375.
What classification code is assigned to this device?
This device is registered under product classification code U01010502.
Similar Classification Devices (U01010502)
Other Devices by Romsons Group Private Limited
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