eudamed_udi
Primary ID: 04719873692026
Carilex (UDI 04719873692026)
Manufactured by CARILEX MEDICAL, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Carilex - Primary ID 04719873692026
Device Regulatory Overview
The Carilex (Model/Catalog Number: S2002-3115) is a medical device manufactured by CARILEX MEDICAL, INC. This product is indexed under FDA Product Code / Category Classification V080701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S2002-3115
- Product Code / EMDN
- V080701
- Device Name
- Anti-decubitus Air Alternating Pressure Device and System with Accessories
- Database Sync Date
- 2026-08-09 16:29:43
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 Carilex?
The registered manufacturer of record for Carilex is CARILEX MEDICAL, INC.
What is the Primary UDI-DI identifier for Carilex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719873692026.
What classification code is assigned to this device?
This device is registered under product classification code V080701.
Similar Classification Devices (V080701)
Other Devices by CARILEX MEDICAL, INC
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