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Highlights from 2023 CMEF – Haobo Imaging together with Detector Technology.
On May 14, the 87th China International Medical Equipment Fair (CMEF) was held in Shanghai. Shanghai Haobo Imaging together with Detection Technology showcased their cutting-edge detector solutions for medical applications. This event attracted global customers, business partners, and ...
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Haobo Imaging’s Successful Debut at 2022CMEF
After many twists and turns, the 86th China International Medical Equipment Fair 2022CMEF grandly opened at the Shenzhen International Convention and Exhibition Center. The first day of the opening was wondeful. Haobo Imaging exhibited a full line of X-ray flat-panel detector products for medical...
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Haobo Imaging sincerely invites you to attend the annual event of CMEF
2022 CMEF——The 86th China International Medical Equipment Fair will be held at Shenzhen International Convention and Exhibition Center from the 23rd to 26th of November 2022. We cordially invite you to Haobo Imaging’s booth at No. 17A31, Hall 17 to connect with our team and explore our state of t...
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Haobo flat panel detector assists in intelligent SMT material management
1.Background In the current Industry 4.0 era, high-efficiency automated production lines are becoming more and more popular. SMT factories have higher requirements for statistical management of materials in and out of the warehouse. It is essential to count materials quickly and accurately. ...
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Basic theory of X-ray machine
Ordinary X-ray machine is mainly composed of console, high-voltage generator, head, table and various mechanical devices. X-ray tube is placed in the head. The high-voltage generator and the head of the small X-ray machine are assembled together, which is called the combined head for its lightne...
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What is the medical device recall?
Medical device recall refers to the behavior of medical device manufacturers to eliminate defects by warning, inspection, repair, re labeling, modifying and improving instructions, software upgrading, replacement, recovery, destruction and other means according to the prescribed ...
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What is the classification of medical device recall?
Medical device recall is mainly classified according to the severity of medical device defects First class recall, the use of the medical device may or has caused serious health hazards. Secondary recall, the use of the medical device may or has caused temporary or reversible health hazards. Thre...
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The latest development of global mainstream flat panel detectors
Canon recently released three Dr detectors at the ahra in Anaheim, California, in July. The lightweight cxdi-710c wireless digital detector and cxdi-810c wireless digital detector have many changes in design and function, including more fillets, tapered edges and built-in grooves for processing a...
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What is the content of the administrative measures for medical device recall (for Trial Implementation)?
Medical device recall refers to the behavior of medical device manufacturers to eliminate defects by warning, inspection, repair, re labeling, modifying and improving instructions, software upgrading, replacement, recovery, destruction and other means according to the prescribed procedures for a ...
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What kind of punishment will be imposed if the medical device fails to fulfill the recall obligation?
If a medical device manufacturer finds a defect in the medical device and fails to recall or refuses to recall the medical device, it shall be ordered to recall the medical device and be fined three times the value of the medical device to be recalled; If serious consequences are caused, the regi...
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What are the requirements of medical device recall?
Medical device manufacturers shall establish and improve the medical device recall system in accordance with the administrative measures for medical device recall (Trial Implementation) issued by the Ministry of health and implemented on July 1, 2011 (Order No. 82 of the Ministry of Health), coll...
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Announcement on active recall of large medical equipment in September 2019
Philips (China) Investment Co., Ltd. reported that due to the products involved, Philips identified a small number of s7-3t and s8-3t Due to the incorrect programming of TEE probe in the manufacturing process,Philips (China) Investment Co., Ltd. made the portable color ultrasound diagnosis system...
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