gudid
Primary ID: ICU008
Invenio (UDI ICU008)
Manufactured by Gri-Alleset, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Invenio - Primary ID ICU008
Device Regulatory Overview
The Invenio (Model/Catalog Number: ICU008) is a medical device manufactured by Gri-Alleset, Inc.. This product is indexed under FDA Product Code / Category Classification LRO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ICU008
- Product Code / EMDN
- LRO
- Device Name
- MST Midline, Maximum Barrier Kit, 5Fr x 10cm
- Database Sync Date
- 2026-08-09 09:07:50
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 Invenio?
The registered manufacturer of record for Invenio is Gri-Alleset, Inc..
What is the Primary UDI-DI identifier for Invenio?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ICU008.
What classification code is assigned to this device?
This device is registered under product classification code LRO.
Similar Classification Devices (LRO)
Other Devices by Gri-Alleset, Inc.
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