Applied Medical Technology IP-1218-S - AMT Initial Placement Gastrostomy Kit With Sheathed Dilator Feeding Tube Device Placement, Each

Part Number Applied Medical Technology IP-1218-S

SKU Number CIA8008811

Sell Unit EACH

Ships Within Call for Availability

List Price $281.18

Product Description

Applied Medical Technology IP-1218-S - AMT Initial Placement Gastrostomy Kit With Sheathed Dilator Feeding Tube Device Placement, Each

AMT Initial Placement Kit

The Initial Placement Kit reduces the trauma associated with stoma tract development. Use laparoscopically, endoscopically or with fluoroscopic guidance. Eliminates a secondary procedure to replace with a low profile. One endoscopic pass reducing trauma.

The AMT I.P. Kits Reduce Trauma Associated with Stoma Tract Development:

Can be used laparoscopically, endoscopically or with fluoroscopic guidance
Requires only one endoscopic pass, reducing trauma
Eliminates the need for a secondary procedure to replace with a low profile device
For use with 12-18F device

AMT Initial Placement Kit Contents (IP-1218-S)

Guidewire (0.038 in dia.)
(1) Introducer Needle 18 gauge
(1) Safety Scalpel #11
(6) Dilators (5, 7, 12, 16, 18 & 22F)
(1) Guidewire Compatible Introducer/Stifener
(1) 5cc Syringe
(1) Guidewire Compatible Balloon Stoma Measuring Device
(4) 4" x 4" Gauze

Includes all the contents of Kit IP-1218, Initial Placement GI Kit EXCEPT the 18F dilator is sheathed.

AMT Initial Placement Kit Anatomy

AMT Offers 3 Initial Placement Kit Options

AMT's Initial Placement Kits (I.P. Kits) provide the essential tools for primary placement of gastrostomy tubes. Our Kits are sterile and ready to go, containing the necessary items to make tube placement easier. The wide variety of dilators, the inclusion of our Balloon Stoma Measuring Device and other kit components put us a step above the rest.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No