gudid
Primary ID: 34-2264-51
ImmunoCAP IgE/ECP/Tryptase Sample Diluent (UDI 34-2264-51)
Manufactured by Phadia AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ImmunoCAP IgE/ECP/Tryptase Sample Diluent - Primary ID 34-2264-51
Device Regulatory Overview
The ImmunoCAP IgE/ECP/Tryptase Sample Diluent (Model/Catalog Number: 34-2264-51) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification DGC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 34-2264-51
- Product Code / EMDN
- DGC
- Device Name
- ImmunoCAP IgE/ECP/Tryptase Sample Diluent
- Database Sync Date
- 2026-08-09 09:48:59
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 ImmunoCAP IgE/ECP/Tryptase Sample Diluent?
The registered manufacturer of record for ImmunoCAP IgE/ECP/Tryptase Sample Diluent is Phadia AB.
What is the Primary UDI-DI identifier for ImmunoCAP IgE/ECP/Tryptase Sample Diluent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 34-2264-51.
What classification code is assigned to this device?
This device is registered under product classification code DGC.
Similar Classification Devices (DGC)
Other Devices by Phadia AB
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