eudamed_udi
Primary ID: 10641043572221
Flow-Safe II (UDI 10641043572221)
Manufactured by Mercury Medical
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flow-Safe II - Primary ID 10641043572221
Device Regulatory Overview
The Flow-Safe II (Model/Catalog Number: 10-57222) is a medical device manufactured by Mercury Medical. This product is indexed under FDA Product Code / Category Classification R03020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-57222
- Product Code / EMDN
- R03020201
- Device Name
- Flow-Safe II
- Database Sync Date
- 2026-08-09 16:50:04
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 Flow-Safe II?
The registered manufacturer of record for Flow-Safe II is Mercury Medical.
What is the Primary UDI-DI identifier for Flow-Safe II?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10641043572221.
What classification code is assigned to this device?
This device is registered under product classification code R03020201.
Similar Classification Devices (R03020201)
Other Devices by Mercury Medical
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