gudid
Primary ID: GIM6000D00
Latitude Catheter (UDI GIM6000D00)
Manufactured by Unisensor AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Latitude Catheter - Primary ID GIM6000D00
Device Regulatory Overview
The Latitude Catheter (Model/Catalog Number: GIM6000D00) is a medical device manufactured by Unisensor AG. This product is indexed under FDA Product Code / Category Classification KLA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GIM6000D00
- Product Code / EMDN
- KLA
- Device Name
- Database Sync Date
- 2026-08-09 09:16:10
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 Latitude Catheter?
The registered manufacturer of record for Latitude Catheter is Unisensor AG.
What is the Primary UDI-DI identifier for Latitude Catheter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GIM6000D00.
What classification code is assigned to this device?
This device is registered under product classification code KLA.
Similar Classification Devices (KLA)
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