gudid
Primary ID: 7100
VitaloJAK (UDI 7100)
Manufactured by VITALOGRAPH (IRELAND) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VitaloJAK - Primary ID 7100
Device Regulatory Overview
The VitaloJAK (Model/Catalog Number: 7100) is a medical device manufactured by VITALOGRAPH (IRELAND) LIMITED. This product is indexed under FDA Product Code / Category Classification DSH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7100
- Product Code / EMDN
- DSH
- Device Name
- Base VitaloJAK UK(1)
- Database Sync Date
- 2026-08-09 09:22:51
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 VitaloJAK?
The registered manufacturer of record for VitaloJAK is VITALOGRAPH (IRELAND) LIMITED.
What is the Primary UDI-DI identifier for VitaloJAK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7100.
What classification code is assigned to this device?
This device is registered under product classification code DSH.
Similar Classification Devices (DSH)
Other Devices by VITALOGRAPH (IRELAND) LIMITED
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