eudamed_udi
Primary ID: 08907265012972
FLEXO CATH (UDI 08907265012972)
Manufactured by Romsons Group Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLEXO CATH - Primary ID 08907265012972
Device Regulatory Overview
The FLEXO CATH (Model/Catalog Number: GS-5034 KAD) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification A0601010401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GS-5034 KAD
- Product Code / EMDN
- A0601010401
- Device Name
- THORACIC DRAINAGE CATHETER (CHEST DRAINAGE CATHETER)
- Database Sync Date
- 2026-08-09 16:29:20
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 FLEXO CATH?
The registered manufacturer of record for FLEXO CATH is Romsons Group Private Limited.
What is the Primary UDI-DI identifier for FLEXO CATH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265012972.
What classification code is assigned to this device?
This device is registered under product classification code A0601010401.
Similar Classification Devices (A0601010401)
Other Devices by Romsons Group Private Limited
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