gudid
Primary ID: MD1-013-01-MOD
Transition Deck (UDI MD1-013-01-MOD)
Manufactured by LIFEPORT, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transition Deck - Primary ID MD1-013-01-MOD
Device Regulatory Overview
The Transition Deck (Model/Catalog Number: MD1-013-01-MOD) is a medical device manufactured by LIFEPORT, LLC. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD1-013-01-MOD
- Product Code / EMDN
- FOX
- Device Name
- ASSEMBLY, TRANSITION DECK, 4G LOCKS
- 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 Transition Deck?
The registered manufacturer of record for Transition Deck is LIFEPORT, LLC.
What is the Primary UDI-DI identifier for Transition Deck?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MD1-013-01-MOD.
What classification code is assigned to this device?
This device is registered under product classification code FOX.
Similar Classification Devices (FOX)
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