gudid
Primary ID: B49558
Beckman Coulter PK Systems Anti-e (P3GD512+MS16+MS21+MS63) (UDI B49558)
Manufactured by DIAGAST
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Beckman Coulter PK Systems Anti-e (P3GD512+MS16+MS21+MS63) - Primary ID B49558
Device Regulatory Overview
The Beckman Coulter PK Systems Anti-e (P3GD512+MS16+MS21+MS63) (Model/Catalog Number: B49558) is a medical device manufactured by DIAGAST. This product is indexed under FDA Product Code / Category Classification within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B49558
- Product Code / EMDN
- N/A
- Device Name
- Blood Grouping Reagent Anti-e (Monoclonal) formulated for Automated Systems, Beckman Coulter PK7400 Systems
- Database Sync Date
- 2026-08-09 10:01:36
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 Beckman Coulter PK Systems Anti-e (P3GD512+MS16+MS21+MS63)?
The registered manufacturer of record for Beckman Coulter PK Systems Anti-e (P3GD512+MS16+MS21+MS63) is DIAGAST.
What is the Primary UDI-DI identifier for Beckman Coulter PK Systems Anti-e (P3GD512+MS16+MS21+MS63)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B49558.
What classification code is assigned to this device?
This device is registered under product classification code .
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