The State Food and Drug Administration recently released the 4th issue of the 2016 medical device quality announcement, in the 193 batches of 6 varieties of medical protective clothing, non-invasive automatic measurement sphygmomanometer ( electronic sphygmomanometer ), blood purification device, etc. When the products were inspected for quality supervision, it was found that the two batches of the four medical device manufacturers had not been in compliance with the standards.
Among them, there are 3 batches of products for 2 medical protective clothing companies. Two batches of medical disposable protective clothing produced by Henan Jianqi Medical Devices Co., Ltd., the appearance and filtration efficiency are not in compliance with the standard; one batch of medical disposable protective clothing produced by Chongyang Wenjian Medical Textile Co., Ltd., appearance and breaking strength Does not meet the standards. Non-invasive automatic measurement sphygmomanometer (electronic sphygmomanometer) 1 company. One BPM series electronic sphygmomanometer produced by Haozhan Medical Technology (Wujiang) Co., Ltd., the color of the button without the light does not meet the standard.
In addition, the items to be tested are medical device products that do not meet the standards as specified in the label, instruction manual, etc., and involve 20 batches (sets) of one medical device manufacturer.
The State Food and Drug Administration requires that relevant medical device manufacturers should conduct risk assessments for products that do not meet the standards and products that do not meet the standards, determine the recall level according to the severity of medical device defects, and actively recall and publicly recall the information. The food and drug supervision and administration department of the enterprise shall supervise the recall of the enterprise, and shall not recall the recall of the organization; if it is found that the medical device product does not meet the standards and cause harm to the human body or there is evidence that it may endanger human health, it may suspend production. Emergency control measures for import, operation and use. Relevant provincial food and drug supervision and administration departments should urge enterprises to ascertain the reasons as soon as possible, formulate corrective measures and rectify them on schedule, and the relevant disposals will be announced to the public before July 30, 2016.
Joist Tape Deck Flashing Tape Butyl Joist Tape for Decking
The Joist Tape is a malleable polyethylene waterproof wood flashing and material, using a rubberized asphalt mastic adhesive. Rot is caused by moisture that stays in contact with treated and untreated lumber deck framing and the above decking material. Wood decay can also occur when deck screws penetrate the deck boards, piercing the joist sub-framing below. The deck joist tape is easily apply to decking joists, around deck support posts and over ledger boards, which creates a waterproof seal that helps stop decay and wood rot.
The joist tape for decking as a barrier, it can reduce moisture damage to crossbeams. The joist butyl tape is used in temperatures range of -20°F to 176°F, it protects and maximizes the life of your new deck and creates a waterproof membrane that prevents wood rot caused by moisture.
Product Name
Material
high-density polyethylene (HDPE)
Adhesive
Pressure Sensitive
PE Film
White, other colors can be customized
Butyl Rubber
white, other colors can be customized
Application
Butyl Joist Tape
Providing corrosion protection
How To Use The Joist Tape for Decking
The joist tape for decking is easy to install just in seconds. Clean the adherend surface, cut the appropriate length as needed, peel off the protected film, and carefully press the tape against target area. Mistakes are easily rectified within the first few minutes of installation.
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