G-Jet® Transgastric-Jejunal Feeding Device
FDA UDIEUDAMEDClass II (US FDA UDI)
Identity
- Trade Name
- AMT G-JET® - Low-Profile Transgastric-Jejunal Feeding Device EUDAMEDG-Jet® Transgastric-Jejunal Feeding Device FDA UDI
- Generic Name
- Gastrojejunostomy tube FDA UDI
- Device Name
- AMT G-JET® EUDAMED14FR x 2.0 cm x 22 cm Low Profile Transgastric-Jejunal Feeding Device, MDR FDA UDI
- Model / Reference
- GJ-1420-22 EUDAMEDFDA UDI
- Description
- 14FR x 2.0 cm x 22 cm Low Profile Transgastric-Jejunal Feeding Device, MDR FDA UDI
Identifiers
- Catalog Number
- GJ-1420-22 FDA UDI
- Primary DI / UDI-DI
- 00842071134082 EUDAMEDFDA UDI
- Basic UDI-DI
- 08420711LOWPROFILEGJETLH EUDAMED
- FDA Product Code
- KNT FDA UDI
- EMDN Code
- G020299 GASTROINTESTINAL FEEDING/ASPIRATION TUBES - OTHER EUDAMED
- GMDN Term
- Gastrojejunostomy tube FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 876.5980 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
Yes
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Dimensions & Sizes
- Size
- Length — 22 Centimeter FDA UDICatheter Gauge — 14 French FDA UDILength — 2.0 Centimeter FDA UDI
Category: Gastrojejunostomy tube
G-Jet® Transgastric-Jejunal Feeding Device by Applied Medical Technology, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED
Similar devices
Also classified as Gastrojejunostomy tube.
- EndoVive Jejunal Feeding Tube — Boston Scientific · Class II
- G-Jet® Transgastric-Jejunal Feeding Device — Applied Medical Technology, Inc. · Class II
- G-Jet® Transgastric-Jejunal Feeding Device — Applied Medical Technology, Inc. · Class II
- Traditional G-Jet® — Applied Medical Technology, Inc. · Class II
- Micro G-Jet® — Applied Medical Technology, Inc. · Class II
- G-Jet® Transgastric-Jejunal Feeding Device — Applied Medical Technology, Inc. · Class II
- G-Jet® Transgastric-Jejunal Feeding Device — Applied Medical Technology, Inc. · Class II
- G-Jet® Transgastric-Jejunal Feeding Device — Applied Medical Technology, Inc. · Class II
Cleared under the same submission
K110804 also covers:
- AMT Guidewire — Applied Medical Technology, Inc.
- AMT Guidewire — Applied Medical Technology, Inc.
- AMT Mini Extension Set — Applied Medical Technology, Inc.
- AMT Mini ONE® Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT Mini™ Extension Set — Applied Medical Technology, Inc.
- AMT Mini™ Extension Set — Applied Medical Technology, Inc.
K123716 also covers:
- AMT Guidewire — Applied Medical Technology, Inc.
- AMT Guidewire — Applied Medical Technology, Inc.
- AMT Mini Extension Set — Applied Medical Technology, Inc.
- AMT Mini ONE® Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT MiniONE Extension Set — Applied Medical Technology, Inc.
- AMT Mini™ Extension Set — Applied Medical Technology, Inc.
- AMT Mini™ Extension Set — Applied Medical Technology, Inc.
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Applied Medical Technology, Inc.
Sources (2)
- FDA UDI 1ed7aa1a-7ecf-4b2b-9ff1-000c159840e6 37 fields · synced Oct 7, 2026
- EUDAMED 9a7a1158-3012-43e9-9943-9e8171710e70 61 fields · synced Oct 7, 2026