BF-730 B5R3 Flow Cytometer (UDI 06935740731607)
Manufactured by URIT Medical Electronic Co.,Ltd.
Device Regulatory Overview
The BF-730 B5R3 Flow Cytometer (Model/Catalog Number: /) is a medical device manufactured by URIT Medical Electronic Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0202040103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W0202040103
- Device Name
- Flow Cytometer
- Database Sync Date
- 2026-08-09 16:46:23
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BF-730 B5R3 Flow Cytometer?
The registered manufacturer of record for BF-730 B5R3 Flow Cytometer is URIT Medical Electronic Co.,Ltd..
What is the Primary UDI-DI identifier for BF-730 B5R3 Flow Cytometer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06935740731607.
What classification code is assigned to this device?
This device is registered under product classification code W0202040103.
Similar Classification Devices (W0202040103)
Other Devices by URIT Medical Electronic Co.,Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint