eudamed_udi
Primary ID: 08906026860104
FLEXIPORT (UDI 08906026860104)
Manufactured by Invent Bio-Med Pvt Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLEXIPORT - Primary ID 08906026860104
Device Regulatory Overview
The FLEXIPORT (Model/Catalog Number: 110805P) is a medical device manufactured by Invent Bio-Med Pvt Ltd. This product is indexed under FDA Product Code / Category Classification A0799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 110805P
- Product Code / EMDN
- A0799
- Device Name
- 2 Port / 3 Port / 4 Port Manifold
- Database Sync Date
- 2026-08-09 16:45:39
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 FLEXIPORT?
The registered manufacturer of record for FLEXIPORT is Invent Bio-Med Pvt Ltd.
What is the Primary UDI-DI identifier for FLEXIPORT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906026860104.
What classification code is assigned to this device?
This device is registered under product classification code A0799.
Similar Classification Devices (A0799)
Other Devices by Invent Bio-Med Pvt Ltd
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