eudamed_udi
Primary ID: 08902141115402
SURU (UDI 08902141115402)
Manufactured by SURU INTERNATIONAL PVT LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SURU - Primary ID 08902141115402
Device Regulatory Overview
The SURU (Model/Catalog Number: 3053.250.60) is a medical device manufactured by SURU INTERNATIONAL PVT LTD. This product is indexed under FDA Product Code / Category Classification A1001010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3053.250.60
- Product Code / EMDN
- A1001010101
- Device Name
- COLOSTOMY BAG
- Database Sync Date
- 2026-08-09 16:29:30
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 SURU?
The registered manufacturer of record for SURU is SURU INTERNATIONAL PVT LTD.
What is the Primary UDI-DI identifier for SURU?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08902141115402.
What classification code is assigned to this device?
This device is registered under product classification code A1001010101.
Similar Classification Devices (A1001010101)
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