gudid
Primary ID: 04
HPH-1000TS HEMOCONCENTRATOR (UDI 04)
Manufactured by MEDICA SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HPH-1000TS HEMOCONCENTRATOR - Primary ID 04
Device Regulatory Overview
The HPH-1000TS HEMOCONCENTRATOR (Model/Catalog Number: 04) is a medical device manufactured by MEDICA SPA. This product is indexed under FDA Product Code / Category Classification KDI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04
- Product Code / EMDN
- KDI
- Device Name
- HPH-1000TS HEMOCONCENTRATOR
- Database Sync Date
- 2026-08-09 09:04:28
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 HPH-1000TS HEMOCONCENTRATOR?
The registered manufacturer of record for HPH-1000TS HEMOCONCENTRATOR is MEDICA SPA.
What is the Primary UDI-DI identifier for HPH-1000TS HEMOCONCENTRATOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04.
What classification code is assigned to this device?
This device is registered under product classification code KDI.
Similar Classification Devices (KDI)
Other Devices by MEDICA SPA
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