pma
Primary ID: P820033
PLASMAFLO (UDI P820033)
Manufactured by Asahi Kasei Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PLASMAFLO - Primary ID P820033
Device Regulatory Overview
The PLASMAFLO (Model/Catalog Number: Unspecified) is a medical device manufactured by Asahi Kasei Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MDP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- MDP
- Device Name
- Separator for therapeutic purposes, membrane automated blood cell/plasma
- Database Sync Date
- 2026-08-09 10:05:00
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 PLASMAFLO?
The registered manufacturer of record for PLASMAFLO is Asahi Kasei Medical Co., Ltd..
What is the Primary UDI-DI identifier for PLASMAFLO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P820033.
What classification code is assigned to this device?
This device is registered under product classification code MDP.
Similar Classification Devices (MDP)
Other Devices by Asahi Kasei Medical Co., Ltd.
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