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What Is A Circumcision Device?

What Is A Circumcision Device?

A Circumcision device is a latest surgical stapler. This device cuts and staples the penile foreskin. It is a revolutionary development in the field of phimosis treatment.
In conventional circumcision, the surgeon has to first cut the skin with a knife and then stitch it. In the circumcision technology, the stitching and the cutting are done by the device. This makes the procedure rapid and painless.
Because of the speed, there is very less bleeding and very less pain to the patient. No surgical stitches are used in the circumcision surgery. The device uses metal clips with silicon ring (figure above).
Our Circumcision stapler has a silicone ring.

Circumcision

  • Painless
  • Stitchless
  • Bloodless
  • Quick 
  • Scarless

Recommended Products

  • Disposable Skin Stapler 35W
  • Staple height: 7.4mm *4.6mm

Main Products

5/5

DISPOSABLE LAPAROSCOPIC  BLADELESS TROCARS

5/5

DISPOSABLE CURVED CUTTER STAPLER (SAME WITH CONTUR)

5/5

DISPOSABLE HEMORRHOIDS STAPLER

5/5

DISPOSABLE ENDOSCOPIC LINEAR CUTTER STAPLER RELOADS

5/5

DISPOSABLE PLASTIBELL CIRCUMCISION DEVICE/STAPLER

5/5

DISPOSABLE LAPAROSCOPIC/ENDOSCOPIC LINEAR CUTTER STAPLER

5/5

DISPOSABLE LINEAR CUTTER STAPLERS (RELOADS WITH BLADE INBUILT)

5/5

DISPOSABLE ENDOSCOPIC RETRIEVAL BAGS

5/5

DISPOSABLE CIRCUMCISION STAPLERS 

5/5

DISPOSABLE LAPAROSCOPIC  OPTICAL TROCARS

5/5

DISPOSABLE SKIN STAPLERS

5/5

DISPOSABLE CIRCUMCISION  STAPLER (WITH SILICONE RUBBER RING)

5/5

DISPOSABLE CIRCULAR  STAPLERS

5/5

DISPOSBALE INCISION RETRACTORS

PRODUCTS FOR COVID-19

Novel Coronavirus (COVID-19) Antigen Detection Kit (Colloidal Gold-Based)

Cassette swab test kits

  • [SPECIFICATIONS]
    20 tests/kit
  • [INTENDED USE]
    The test kit is applicable to detect the antigen of Novel Coronavirus (COVID-19) Antigen in human throat swab, Nasal swab samples.
  • [INTERPRETING TEST RESULTS]
    The test results are analyzed as follows:

Novel Coronavirus (COVID-19) Nucleic Acid Detection Kit (Fluorescence RT-PCR)

  • [SPECIFICATIONS]
    48 tests / kit
  • [INTENDED USE]
    This kit is used for the qualitative detection of novel coronavirus (COVID-19) ORF1ab gene and N gene in the nasopharyngeal swabs、sputum and alveolar lavage fluid samples, which might from those suspected cases of COVID-19 infection, suspected clustered patients, and other patients who need to be diagnosed with COVID-19.
  • [SAMPLE REQUIREMENTS]
    Applicable sample types: Nasopharyngeal swabs,
    Sputum, Alveolar lavage fluid samples, Virus
    preservation solution or RNA preservation solution.
  • SAMPLE COLLECTION:
    1.Collected samples in sterile tubes.
    2.Swabs: Swab the nasal cavity or pharyngeal
    secretion with sterile swab, place it in the Sample preservation solution.
    3.Sputum: Rinse the mouth with clear water 3 times
    before taking, and forcefully cough up the sputum in
    the deep respiratory tract and spit it into the sterile
    sputum collector. When the patient’s sputum is deep and hard to be expectorated, they can beat their backs
    4.Alveolar lavage fluid samples: Collect the
    bronchoalveolar lavage fluid and store it in airtight package.
  • [REQUIRED EQUIPMENT]
    Quantitative PCR instrument: supports FAM, VIC,
    fluorescence channel.
    Model:ABI 7500,Roche lightcycle 480, etc.

Novel Coronavirus (COVID-19) Neutralizing Antibody Detection Kit(Colloidal Gold-Based)

  • [SPECIFICATION]
    20 tests/kit
  • [INTENDED USE]
    The kit is used for qualitative evaluation of the level of neutralizing antibody in human after being vaccinated with COVID-19 vaccine and recovering from infection. Test samples include human serum, plasma, fingertip blood and venous whole blood.
  • [DETECTION PRINCIPLE]
    The immunochromatographic principle of the kit is applied to detect neutralizing antibody in COVID-19 by competitive method. When the test sample contains neutralizing antibody in human after being vaccinated with COVID-19 vaccine and recovering from infection and the concentration is not lower than the minimum detection limit, neutralizing antibody bind to the marker, and the T-line (S-RBD antibody) in the detection area has no binding substance and does not form a red reaction line, the result is positive. On the contrary, when the red band is displayed, the result is negative. Under normal test conditions, the C-line (internal reference antibody) in the quality control area shows red band, indicating that the test is effective.
  • [SAMPLE REQUIREMENTS]
    1.Whole blood, serum or plasma samples are collected by EDTA anticoagulant tubes.

[TEST RESULT]

EC Certificates

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 UPWELL MEDICAL CO., LTD.

   EMAIL ADDRESS:

  • INFO@UPWELLMEDICAL.COM

  • INFO@UPWELLMED.COM

  • LEE@UPWELLMED.COM