Mycoplasma Pneumoniae Culture Identification and Susceptibility Kit

Mycoplasma Pneumoniae Culture Identification and Susceptibility Kit Instruction

[Package Specification]

20pcs/box

[IntendedUse]

It is used for culture, identification and drug sensitivity test of mycoplasma pneumoniae.

Mycoplasma pneumoniae (MP) is a microorganism between virus and bacteria, which is small and larger than viruses. It is the smallest prokaryote that can reproduce itself, but at the same time it has some characteristics of bacteria with DNA and RNA but without cell wall. MP is the pathogen of human mycoplasma pneumonia and one of the main pathogens causing respiratory tract infection and atypical pneumonia in children. More than 1 / 3 of non-bacterial pneumonia are caused by MP infection, which clinical manifestations of is mainly respiratory symptoms.

[Test Method]

1. Take the required amount of medium and restore to room

temperature (20 ~ 30℃).

2. Add 100μl culture medium into Al blank hole, and then add 1 drop

of liquid paraffin oil.

3. Inoculating secretion sample: insert the sample collected by

sterile swab into the culture medium, squeeze the rotary swab several times to make the sample in the swab infiltrate and discard the swab.

4. Fully mix the liquid medium inoculated with the sample, and

accurately measure 100 μl of the sample by sampler into the remaining holes of the drug sensitive plate (except A1).

5. After adding the medium, drip 1 drop of paraffin oil (about 50

μL) into each hole of the drug sensitive plate, and then cover it.

6. The remaining medium is incubated in 37℃ incubator

together with the drug sensitive plate, and the results are observed in 48 ~ 72 hours.

【Company Information】

Name of Registrant/ Manufacturer： Zhuhai Langfeng Biotechnology Co., Ltd

Address：Building 4, Chengyuwei

Industrial Zone, Baijiao Town, Doumen District, Zhuhai City

Telephone：0756-5503964

Name of After

Sales Service Unit：Zhuhai Langfeng Biotechnology Co., Ltd

Telephone：0756-6256305

Addressof Manufacturing ：Building 4, Chengyuwei Industrial Zone, Baijiao Town, Doumen District,

Zhuhai City

Production license number：Guangdong Food and Drug Administration to the Production of Xu 20162751

【Medical Device Registration Certificate Number/ Product Technical Requirement No】China  Mechanical Note 20172401687

【Date of Approval and Revision】October 9, 2017