The umbilical cord can be removed 24 hours postpartum or as ordered by the doctor

Neonatal umbilical cord clip, also known as disposable umbilical cord clipper, is a one-time use umbilical cord clipper, suitable for cutting and separation of neonatal umbilical cord and comprehensive umbilical care. Function 2 of the umbilical cord clamp: In terms of time and speed, a single person can easily complete the expectant treatment of the newborn in just 2 seconds, which greatly shortens the working time of medical staff; The third function of the umbilical cord clip: reduce the blood exposure of medical staff in the delivery room environment, and also allow each person to receive the best care at the moment of birth.

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Disposable forceps of the utility model have strong practical value

The utility model relates to a pair of forceps, in particular to a disposable medical long forceps. It belongs to the field of medical devices. Traditional medical forceps are mostly made of stainless steel or copper alloy materials, which are usually repeated and can be reused. The medical forceps are basically like scissors in structure, the middle is the fulcrum, and the two ends are the handle and the forceps feet respectively. However, in some medical and surgical fields, long forceps are often required, such as gynecology. Traditional forceps are not practical due to insufficient length and too large handle opening angle.

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What is the classification of medical device product changes?

1. The contents stated in the registration certificate, including product name, model, specification, structure and composition, scope of application, product technical requirements, production address of imported medical devices, etc. This type of change belongs to the change of the license item, and an application for change registration should be submitted to the original registration department. Generally, technical review and administrative approval are required. If there is a substantial change, an on-site assessment is also required. 2. The contents stated in the registration certificate, including the name and domicile of the registrant, the name and domicile of the agent, and the house number of the production address, etc. This type of change belongs to the change of the registration item, and the original registration department should apply for the record of the change item

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What are the requirements for imported medical devices? Pay attention to the following 4 aspects

1. The imported medical devices should be registered or filed medical devices, and the medical device registration certificate is valid for 5 years. If it is necessary to renew the registration after the expiry of the validity period, an application for renewal of the registration shall be submitted to the original registration department 6 months before the expiry of the validity period. 2. The customs conducts online verification of the electronic data of the imported medical device record/registration certificate (including the medical device registration certificate, the first-class medical device record certificate) and the electronic data of the imported medical device product declaration form. The contract, invoice, packing list, and medical device filing/registration certificate should be provided when importing medical devices for customs declaration.

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What problems should you pay attention to when buying home medical equipment online?

1. Online shopping of medical devices is based on the "three certificates" 1. Look at the medical device product certificate. Medical device products must obtain a medical device registration certificate or filing certificate in accordance with the law. Consumers can log in to the “Data Inquiry” and “Medical Devices” columns of the National Drug Administration website to inquire about medical device related information. 2. Look at the production enterprise certificate. The production of medical devices requires a medical device production license and a record certificate. 3. Look at the business certificate. The operation of Class III medical devices requires a medical device operation license; the operation of Class II medical devices requires an operation record certificate. 4. Online sales of medical devices must follow the principle of "consistency between online and offline": companies that sell medical devices online must have physical stores offline, and their business scope must be the same as that of physical stores. Individuals or individual industrial and commercial households are not allowed to sell medical devices online.

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Medical device instructions and labels should indicate these points

1. Common name, model, specification; 2. The name, address and contact information of the medical device registrant, filing person, and entrusted manufacturer; 3. Date of manufacture, expiry date or expiration date; 4. Product performance, main structure, scope of application; 5. Taboos, precautions and other content that needs warning or prompting; 6. Installation and use instructions or illustrations; 7. Maintenance and maintenance methods, special conditions and methods of transportation and storage; 8. Other contents that should be marked in the technical requirements of the product.

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