eudamed_udi
Primary ID: 08885020070033
ArmFlow (UDI 08885020070033)
Manufactured by ARTICARES PTE LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ArmFlow - Primary ID 08885020070033
Device Regulatory Overview
The ArmFlow (Model/Catalog Number: NA) is a medical device manufactured by ARTICARES PTE LTD. This product is indexed under FDA Product Code / Category Classification Z12069080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NA
- Product Code / EMDN
- Z12069080
- Device Name
- ArmFlow
- Database Sync Date
- 2026-08-09 16:48:35
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 ArmFlow?
The registered manufacturer of record for ArmFlow is ARTICARES PTE LTD.
What is the Primary UDI-DI identifier for ArmFlow?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08885020070033.
What classification code is assigned to this device?
This device is registered under product classification code Z12069080.
Similar Classification Devices (Z12069080)
Other Devices by ARTICARES PTE LTD
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