eudamed_udi
Primary ID: G573T7119B1
Umaflow (UDI G573T7119B1)
Manufactured by ROYAL SURGICARE PRIVATE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Umaflow - Primary ID G573T7119B1
Device Regulatory Overview
The Umaflow (Model/Catalog Number: T-7119/B) is a medical device manufactured by ROYAL SURGICARE PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification A99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T-7119/B
- Product Code / EMDN
- A99
- Device Name
- Blood Transfusion Set
- Database Sync Date
- 2026-08-09 16:49:12
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 Umaflow?
The registered manufacturer of record for Umaflow is ROYAL SURGICARE PRIVATE LIMITED.
What is the Primary UDI-DI identifier for Umaflow?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G573T7119B1.
What classification code is assigned to this device?
This device is registered under product classification code A99.
Similar Classification Devices (A99)
Other Devices by ROYAL SURGICARE PRIVATE LIMITED
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