GUDIDData
gudid Primary ID: TBC003

Invenio (UDI TBC003)

Manufactured by GRI Medical & Electronic Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Invenio - Primary ID TBC003

Device Regulatory Overview

The Invenio (Model/Catalog Number: TBC003) is a medical device manufactured by GRI Medical & Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification PXI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TBC003
Product Code / EMDN
PXI
Device Name
Breast Pack_Sterile_4EA/CS
Database Sync Date
2026-08-09 09:22:01

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

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 Medical & Electronic Technology Co., Ltd..

What is the Primary UDI-DI identifier for Invenio?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TBC003.

What classification code is assigned to this device?

This device is registered under product classification code PXI.

Similar Classification Devices (PXI)

Other Devices by GRI Medical & Electronic Technology Co., Ltd.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint