Benefits
1,Super softness and patient comfort.
2,High absorbency, less neps.
3,Quick absorbent capability.
4,Available in various sizes.
Indication
Cotton roll is ideal for wound cleansing, application of medication, and packing of wound area and also apply astringents; remove makeup and nail polish; facial wash pad; baby care.
Sizes
Â
REF NO. | Spec. | Packaging |
403 001 | 25g | 1roll/pack, 200pks/case |
403 002 | 50g | 1roll/pack, 200pks/case |
403 003 | 100g | 1roll/pack, 100pks/case |
403 004 | 400g | 1roll/pack, 30pks/case |
403 005 | 450g | 1roll/pack, 30pks/case |
403 006 | 500g | 1roll/pack, 30pks/case |
403 007 | 1000g | 1roll/pack, 12pks/case |
403 008 | 500g, with interleaf | 1roll/pack, 30pks/case |
 Medical Absorbent BP Cotton Wool is soft, absorbent and 100% bleached cotton roll wrapped in paper. Cotton roll can be cut to any shapes and sizes, has wide range of applications for medical usage, meet with BP standards.
Benefits
1,Super softness and patient comfort.
2,High absorbency, less neps.
3,Quick absorbent capability.
4,Available in various sizes.
Indication
Cotton roll is ideal for wound cleansing, application of medication, and packing of wound area and also apply astringents; remove makeup and nail polish; facial wash pad; baby care.
Sizes
Â
REF NO. | Spec. | Packaging |
403 001 | 25g | 1roll/pack, 200pks/case |
403 002 | 50g | 1roll/pack, 200pks/case |
403 003 | 100g | 1roll/pack, 100pks/case |
403 004 | 400g | 1roll/pack, 30pks/case |
403 005 | 450g | 1roll/pack, 30pks/case |
403 006 | 500g | 1roll/pack, 30pks/case |
403 007 | 1000g | 1roll/pack, 12pks/case |
403 008 | 500g, with interleaf | 1roll/pack, 30pks/case |
Â
The RT-PCR Test Reagent Kit is a real-time, RT-PCR test intended for the qualitative detection of nucleic acid from SARS-CoV-2 in oropharyngeal and nasopharyngeal swab specimens from individuals suspected of COVID-19 by their healthcare provider. This test is also for use with anterior nasal swab specimens that are collected using the COVID-19 Test Collection Kit when used consistent with its authorization.
Results are for the identification of SARS-CoV-2 RNA. The SARS-CoV-2 RNA is generally detectable in the upper respiratory specimens during the acute phase of infection.
Positive results are indicative of the presence of SARS-CoV-2 RNA; clinical correlation with patient history and other diagnostic information is necessary to determine patient infection status.
Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.
Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. Negative results must be combined with clinical observations,patient history,and epidemiological information.
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