Injection Site Adapter--Guangdong Baihe Medical Technology Co., Ltd.

Injection Site Adapter

The ABLE® Injection Site Adapter is made of medical grade polycarbonate (PC) and synthetic rubber materials, and the tube part is made of polyurethane. The ordinary type is composed of a base (conical fitting) injection molded rubber pad, while the needle free type is composed of an injection seat, piston, and conical connector. The tube type consists of a tube and an infusion connector. The connection port of the base is a 6:100 ruhr conical connector. The needle free infusion connector has a positive pressure feeding function.

Intended Use
Order Information
Contraindication
Warning and Precautions

The product is used to close the transfusion port, supply liquid medicine when the adaptor is closed and prevent the transfusion system from polluting during intravenous infusion therapy.

Disposable Injection Site Adapter
Type	Specification
Normal adapter	Normal adapter CVC
	Normal adapter E
	Normal adapter D
Needle free connector	Needle free connector I
	Needle free connector Y
	Y-port valves needle free connector I
	Needle free connector I with connected catheter
	Needle free connector AL
	Needle free connector AP
	Needle free connector L
	Needle free connector O
Injection site adapter with extension tubes	Needle free connector VI
	Needle free connector CL
	Needle free connector GL
	Needle free connector IV
	Needle free connector BL
	Needle free connector BP
	Needle free connector VII
	Needle free connector DL
	Needle free connector CP
	Needle free connector EL
	Needle free connector DP
	Needle free connector VIII
	Needle free connector FL
	Needle free connector EP

No absolute contraindication.

Warning:
1. Do not use the product when the package is damaged.

2. The validity period is 36 months.

3. The ordinary infusion connector (heparin cap) needs to be replaced daily and used for no more than 24 hours each time; The expected continuous use time of the needle free infusion connector shall not exceed 7 days, with a total of no more than 56 times, whichever occurs first, and the connector shall be replaced according to regulations; The expected usage time of the infusion connector with tubing (ordinary type, i.e. heparin cap) shall not exceed 24 hours, and the expected continuous usage time of the infusion connector with tubing (needle free type) shall not exceed 7 days, for a total of 56 times.

4. If there any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.

Precautions:

1. Single use only, do NOT reuse. Reuse can lead to serious inflammation or inflection even death.

2. Dispose of the device as a contaminated medical device and in accordance with hospital protocols.

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