gudid
Primary ID: 100-6341-02
AeroSled Transport Deck (TD) (UDI 100-6341-02)
Manufactured by LIFEPORT, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AeroSled Transport Deck (TD) - Primary ID 100-6341-02
Device Regulatory Overview
The AeroSled Transport Deck (TD) (Model/Catalog Number: 100-6341-02) 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
- 100-6341-02
- Product Code / EMDN
- FOX
- Device Name
- AEROSLED TD (ASTAR 300 LB) * TRANSPORT DECK
- 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 AeroSled Transport Deck (TD)?
The registered manufacturer of record for AeroSled Transport Deck (TD) is LIFEPORT, LLC.
What is the Primary UDI-DI identifier for AeroSled Transport Deck (TD)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 100-6341-02.
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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