gudid
Primary ID: MP2-013-01
MedPak (UDI MP2-013-01)
Manufactured by LIFEPORT, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MedPak - Primary ID MP2-013-01
Device Regulatory Overview
The MedPak (Model/Catalog Number: MP2-013-01) is a medical device manufactured by LIFEPORT, LLC. This product is indexed under FDA Product Code / Category Classification BTI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MP2-013-01
- Product Code / EMDN
- BTI
- Device Name
- ASSEMBLY, MEDPAK, LIGHTWEIGHT
- Database Sync Date
- 2026-08-09 09:10:00
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 MedPak?
The registered manufacturer of record for MedPak is LIFEPORT, LLC.
What is the Primary UDI-DI identifier for MedPak?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MP2-013-01.
What classification code is assigned to this device?
This device is registered under product classification code BTI.
Similar Classification Devices (BTI)
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