gudid
Primary ID: 2120
2120 In2itive - Brazil (UDI 2120)
Manufactured by VITALOGRAPH (IRELAND) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 2120 In2itive - Brazil - Primary ID 2120
Device Regulatory Overview
The 2120 In2itive - Brazil (Model/Catalog Number: 2120) is a medical device manufactured by VITALOGRAPH (IRELAND) LIMITED. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2120
- Product Code / EMDN
- BZG
- Device Name
- Database Sync Date
- 2026-08-09 09:57:29
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 2120 In2itive - Brazil?
The registered manufacturer of record for 2120 In2itive - Brazil is VITALOGRAPH (IRELAND) LIMITED.
What is the Primary UDI-DI identifier for 2120 In2itive - Brazil?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2120.
What classification code is assigned to this device?
This device is registered under product classification code BZG.
Similar Classification Devices (BZG)
Other Devices by VITALOGRAPH (IRELAND) LIMITED
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