gudid
Primary ID: 10-9413-01
ImmunoCAP Thyroglobulin IgG Antibodies Control NLH (UDI 10-9413-01)
Manufactured by Phadia AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ImmunoCAP Thyroglobulin IgG Antibodies Control NLH - Primary ID 10-9413-01
Device Regulatory Overview
The ImmunoCAP Thyroglobulin IgG Antibodies Control NLH (Model/Catalog Number: 10-9413-01) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification JJY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-9413-01
- Product Code / EMDN
- JJY
- Device Name
- Contains 2 vials of each IgG antibodies level (N: normal; L: low; H: high) for the ImmunoCAP Thyroglobulin method.
- 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 Thyroglobulin IgG Antibodies Control NLH?
The registered manufacturer of record for ImmunoCAP Thyroglobulin IgG Antibodies Control NLH is Phadia AB.
What is the Primary UDI-DI identifier for ImmunoCAP Thyroglobulin IgG Antibodies Control NLH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-9413-01.
What classification code is assigned to this device?
This device is registered under product classification code JJY.
Similar Classification Devices (JJY)
Other Devices by Phadia AB
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