gudid
Primary ID: CPK-310A
CELLPACK (UDI CPK-310A)
Manufactured by SYSMEX CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CELLPACK - Primary ID CPK-310A
Device Regulatory Overview
The CELLPACK (Model/Catalog Number: CPK-310A) is a medical device manufactured by SYSMEX CORPORATION. This product is indexed under FDA Product Code / Category Classification GIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CPK-310A
- Product Code / EMDN
- GIF
- Device Name
- Whole blood diluent for use in hematology analyzers
- Database Sync Date
- 2026-08-09 09:17:27
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 CELLPACK?
The registered manufacturer of record for CELLPACK is SYSMEX CORPORATION.
What is the Primary UDI-DI identifier for CELLPACK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CPK-310A.
What classification code is assigned to this device?
This device is registered under product classification code GIF.
Similar Classification Devices (GIF)
Other Devices by SYSMEX CORPORATION
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