gudid
Primary ID: E3-2412
Decompression Tube (UDI E3-2412)
Manufactured by APPLIED MEDICAL TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Decompression Tube - Primary ID E3-2412
Device Regulatory Overview
The Decompression Tube (Model/Catalog Number: E3-2412) is a medical device manufactured by APPLIED MEDICAL TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification KGC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E3-2412
- Product Code / EMDN
- KGC
- Device Name
- 24F x 1.2 cm Decompression Tube (Pouched)
- Database Sync Date
- 2026-08-09 09:50:43
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 Decompression Tube?
The registered manufacturer of record for Decompression Tube is APPLIED MEDICAL TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for Decompression Tube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E3-2412.
What classification code is assigned to this device?
This device is registered under product classification code KGC.
Similar Classification Devices (KGC)
Other Devices by APPLIED MEDICAL TECHNOLOGY, INC.
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