gudid
Primary ID: 100-5721-03
MedPak (UDI 100-5721-03)
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 100-5721-03
Device Regulatory Overview
The MedPak (Model/Catalog Number: 100-5721-03) 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
- 100-5721-03
- Product Code / EMDN
- BTI
- Device Name
- MEDPAK ASSEMBLY
- Database Sync Date
- 2026-08-09 09:10:00
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 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 100-5721-03.
What classification code is assigned to this device?
This device is registered under product classification code BTI.
Similar Classification Devices (BTI)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint