gudid
Primary ID: AS1-001-04
AeroSled Turbo Sled (TS) (UDI AS1-001-04)
Manufactured by LIFEPORT, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AeroSled Turbo Sled (TS) - Primary ID AS1-001-04
Device Regulatory Overview
The AeroSled Turbo Sled (TS) (Model/Catalog Number: AS1-001-04) is a medical device manufactured by LIFEPORT, LLC. This product is indexed under FDA Product Code / Category Classification FPP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AS1-001-04
- Product Code / EMDN
- FPP
- Device Name
- AEROSLED TS
- 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 Turbo Sled (TS)?
The registered manufacturer of record for AeroSled Turbo Sled (TS) is LIFEPORT, LLC.
What is the Primary UDI-DI identifier for AeroSled Turbo Sled (TS)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AS1-001-04.
What classification code is assigned to this device?
This device is registered under product classification code FPP.
Similar Classification Devices (FPP)
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