Name: F2394-X2.2 Standard Test Vessel Model
Brand: Preclinic Medtech (Shanghai) Co., Ltd.
Availability: InStock

F2394-X2.2 Standard Test Vessel Model

Made according to ASTM F 2394-07 (2022) standard, used for particle testing of drug delivery devices and drug transfer testing

Specification of F2394-X2.2 Standard Test Vessel Model

Fetures	Strictly designed and manufactured according to ASTM F2394-07 standard, 1:1 accurate simulation of coronary artery lumen size ensures high compatibility between vessel morphology, size and standard test requirements, providing an authoritative and reliable simulation environment for interventional device testing. The main body is made of highly transparent soft silicone gel (transparency ≥ 90%), which can clearly observe the movement trajectory and operation status of instruments such as guide wires, catheters, balloon stents, etc. inside the blood vessels, facilitate real-time evaluation of instrument performance, standardize surgical operation procedures, and enhance the intuitiveness of training and testing.
PN	PLJTXG002
NW	0.4KG
Main Material	Highly transparent soft silica gel, hardness: 30A, or acrylic.
Product Size	Model length: 28 cm
	Model width: 15 cm
	Model height: 2 cm
Lead Time	15 days
Origin	Shanghai, China

FAQ On Drawing of F2394-X2.4 Standard Test Vessel Model_copy20260109165708

Q: What intervention instrument testing and surgical training programs does this experimental model support?

A: Support performance testing and evaluation of vascular intervention devices such as guide catheters, guide wires, balloon dilation stents, etc; Simulation training for vascular angiography surgery and balloon dilation surgery can be conducted to accurately match the equipment validation and basic operation training needs in the field of coronary intervention.

Q: What standards does the model meet? What does this mean for use?

A: The model is designed and manufactured strictly in accordance with ASTM F2394-07 standard. This standard is an authoritative reference for the testing of vascular intervention devices. Compliance with this standard means that the core parameters of the model, such as vessel size and shape, have standardization and uniformity, providing a comparable and reliable simulation environment for device testing, ensuring the accuracy and authority of test results.