Procleix Auto Detect Reagents (UDI 00850032683579)
Manufactured by Grifols Diagnostic Solutions Inc.
Device Regulatory Overview
The Procleix Auto Detect Reagents (Model/Catalog Number: 9053575) is a medical device manufactured by Grifols Diagnostic Solutions Inc.. This product is indexed under FDA Product Code / Category Classification W01019001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9053575
- Product Code / EMDN
- W01019001
- Device Name
- Procleix Auto Detect Reagents
- Database Sync Date
- 2026-08-09 17:34:11
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 Procleix Auto Detect Reagents?
The registered manufacturer of record for Procleix Auto Detect Reagents is Grifols Diagnostic Solutions Inc..
What is the Primary UDI-DI identifier for Procleix Auto Detect Reagents?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850032683579.
What classification code is assigned to this device?
This device is registered under product classification code W01019001.
Similar Classification Devices (W01019001)
Other Devices by Grifols Diagnostic Solutions Inc.
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