eudamed_udi
Primary ID: 06935740718530
URIT D31 Diluent (UDI 06935740718530)
Manufactured by URIT Medical Electronic Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URIT D31 Diluent - Primary ID 06935740718530
Device Regulatory Overview
The URIT D31 Diluent (Model/Catalog Number: /) is a medical device manufactured by URIT Medical Electronic Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0103010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W0103010105
- Device Name
- Diluent
- Database Sync Date
- 2026-08-09 16:49:15
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 URIT D31 Diluent?
The registered manufacturer of record for URIT D31 Diluent is URIT Medical Electronic Co.,Ltd..
What is the Primary UDI-DI identifier for URIT D31 Diluent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06935740718530.
What classification code is assigned to this device?
This device is registered under product classification code W0103010105.
Similar Classification Devices (W0103010105)
Other Devices by URIT Medical Electronic Co.,Ltd.
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