gudid
Primary ID: 31405.45
INKA (UDI 31405.45)
Manufactured by The Trustee for KAISER FAMILY TRUST
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INKA - Primary ID 31405.45
Device Regulatory Overview
The INKA (Model/Catalog Number: 31405.45) is a medical device manufactured by The Trustee for KAISER FAMILY TRUST. This product is indexed under FDA Product Code / Category Classification JYJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 31405.45
- Product Code / EMDN
- JYJ
- Device Name
- HOUSE Measuring Rod 4.5mm 16cm
- Database Sync Date
- 2026-08-09 09:38:28
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 INKA?
The registered manufacturer of record for INKA is The Trustee for KAISER FAMILY TRUST.
What is the Primary UDI-DI identifier for INKA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 31405.45.
What classification code is assigned to this device?
This device is registered under product classification code JYJ.
Similar Classification Devices (JYJ)
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