eudamed_udi
Primary ID: D-08885020070002Q3
H-MAN (UDI D-08885020070002Q3)
Manufactured by ARTICARES PTE LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for H-MAN - Primary ID D-08885020070002Q3
Device Regulatory Overview
The H-MAN (Model/Catalog Number: NA) is a medical device manufactured by ARTICARES PTE LTD. This product is indexed under FDA Product Code / Category Classification Z120616 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NA
- Product Code / EMDN
- Z120616
- Device Name
- H-MAN
- Database Sync Date
- 2026-08-09 17:29:06
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 H-MAN?
The registered manufacturer of record for H-MAN is ARTICARES PTE LTD.
What is the Primary UDI-DI identifier for H-MAN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-08885020070002Q3.
What classification code is assigned to this device?
This device is registered under product classification code Z120616.
Similar Classification Devices (Z120616)
Other Devices by ARTICARES PTE LTD
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