Surgical Products

• Strong adhesive ensures a secure fit.
• Skin-friendly material.
• It is flexible and is suitable for sizes upto 60 mm.
• Belt loops are provided.

• Production Capacity: 200
• Delivery Time: week
• Packaging Details: 5 pieces in one box

Smiths Medical''s popular JELCO® I.V. Catheter is a leading conventional peripheral I.V. catheter. The FEP polymer construction and "J"-point needle design allow clinicians to easily feel the vein entry. Anesthesiologists rely on JELCO® I.V. Catheters for their ease of use starting arterial lines and gaining I.V. access. The thin wall catheter design provides higher flow rates than standard wall catheters, often allowing for use in a smaller gauge device.

• Item Code: 4035
• Production Capacity: 200 Boxes
• Delivery Time: Within 7 Days
• Packaging Details: Export Worth Corrugated Box Packing

- Needle Length: 26mm

- Suture Length: 100cm

- Colour: Green

- Suture Type: Synthetic Braided

- Absorption Profile: Non Absorbable

- Suture Diameter: USP 3-0

- Suture Material: Polyester - Poly (ethylene terephthalate)

- Coating: Polybutilate

- Needle Description: 26mm, 1/2 Circle Round Body

- Tensile Strength: Indefinite Breaking Strength Retention

• Production Capacity: 100 box
• Delivery Time: 7 DAYS
• Packaging Details: 12 FOILS IN ONE BOX

Directions for Use

There are similarities between sterilization inks and other graphic printing inks. However, there are differences that impact the inks performance. For example; to achieve the signal change of the Chemical Indicator, the amount of ink typically required is greater than the ink printed for the same size graphic image. Please follow provided guidelines and contact our technical support for additional assistance.

1. Bring ink to room temperature before printing.

2. Thoroughly mix ink until fully homogeneous, ensuring that all solids are incorporated in the solution.

3. A recommended thinner may be added for adjusting viscosity up to 5% at a time:

   Note: Thinning the ink may impact functionality. Confirm initial and signal colors with each thinner addition.
   Thinner: Distilled Water

4. Do not mix in any additives as they may interfere with the chemical reaction that causes the color change; contaminants risk changing the ink chemistry.

5. Be sure to wash all cleaning fluid off any area of print press that will contact ink; cleaning fluids can cause ink chemistry change.

6. Ensure that during the printing process, ink in the fountain is stirred continuously to avoid solids depositing on the bottom of the tray.

7. Viscosity should be monitored on a regular basis, typically 30 to 60 minute intervals.

8. Use best quality substrates.

9. Always run a sterilization test prior to a full run.

10. Itiscriticaltoensuresufficientinklaydowninorderfortheconvertedchemicalindicatortoperformas

    intended.

     

    Performance Conditions
    a. Thirty (30) min +/- 15 s, 30°C/86°F +/-1°C, Gas concentration 600 mg +/-30 mg, RH 60% +/-10%, OR b. Twenty (20) min +/-15 s, 54°C/129°F +/-1°C, Gas concentration 600 mg +/-30 mg, RH 60% +/-10%

    Recommended Usage Period

    Six (6) months from date of shipment when stored as recommended.

    Storage & Handling

    · Store Ink in the original closed container in a cool and dry place between 60° F/15°C and 80°F/27°C; do not freeze.

    · Refer to Safety Data Sheet for information on handling and safety instructions.

    Warranty

    LA-CO Industries (LA-CO) agrees to exchange or refund the price of Tempil inks which, at LA-COs discretion, contain material and/or manufacture defects, when stored in the original container in the recommended storage conditions. There is no guarantee or warranty as to anything made or sold by LA-CO, or of any services performed except as to title and freedom from encumbrances and except as herein expressly stated and particularly, and without limit the foregoing, there is no guarantee or warranty, express or implied, or merchantability or of fitness for any particular purpose or against claim of infringement or the like. LA-CO makes no warranty (and assumes no liability) as to function of product or systems built to Buyers design or of the ability of any goods to interface, operate or function with any portions of Buyers system not provided by LA-CO.

• Item Code: TIGFAC564A
• Production Capacity: 5000
• Delivery Time: Within 2 weeks
• Packaging Details: Export worth packing

Catalog # : 544250 Weck ® Hem-o-lok ® Polymer Ligating  product › 5...  

• Production Capacity: 50 BOX
• Delivery Time: 7 Days
• Packaging Details: 14 CARTRIDGE IN ONE BOX

1. Hem-o-lok. Weck Web Catalog. TESTIMONIALS. Rarely is a product so perfectly matched with an indication as exists with the Hem-o-Lok and Cholecystectomy. There is no clip on the market more reliable for cystic duct and artery clipping. The various clip size options, as well as variable applicator shaft lengths, make it an ideal solution for any circumstance, including the incidental cholecystectomy done concurrently with other procedures including bariatric surgery.

• Production Capacity: 50 BOX
• Delivery Time: 7 DAYS
• Packaging Details: 14 CARTRIDGE IN ONE BOX

Leukotape® classic stabilizes both mechanically and proprioceptively. Offering outstanding user comfort, its high adhesive strength ensures the non-slip fit of the tape bandage

Wide range of benefits for you and your patientsReliable fit

• adheres reliably to the skin and underlay material
• also adheres securely under strain
• particularly high tensile strength

High user comfort

• skin-friendly, made of 100 % cotton fabric
• dirt and water repellent

Easy to use

• the rounded edges of the plastic core reduce the risk of injury and allow the tape to be unrolled up to the last centimetre
• can be torn lengthwise and crosswise, allowing individual application without scissors

Long lasting

• the bandage remains in place for several days, saving time and costs

In attractive colours

• comes in white and five colors
• matches sports outfits

Main uses

• for functional bandaging of injuries to muscles, ligaments and joints
• for protecting already damaged joints against injury 

• Item Code: 01703
• Production Capacity: 5000
• Delivery Time: within 2 weeks
• Packaging Details: Export worth packing

Welcome to BSN medical

BSN medical is a global leader in the worldwide healthcare market specialising in the areas of Compression Therapy, Wound Care and Orthopaedics. We are focused on the development of world-class branded products that offer high quality solutions for our caregivers and patients.

BSN medical connects its broad portfolio in Wound Care & related Vascular Diseases, Lymphology and non-invasive Orthopaedics with strong technological competencies to meet the market's need for reduced complexity and more efficient treatments. With a continuously developing unique and holistic network of integrated therapy solutions, BSN medical consistently supports a continuum of care.

Welcome to Therapies. Hand in Hand.
Welcome to Integrated Therapy Solutions.

In April 2017, BSN medical was acquired by Swedish Essity AB (former SCA), a leading global hygiene and health company that develops, produces and sells Personal Care (Baby Care, Feminine Care, Incontinence Products and Medical Solutions), Consumer Tissue and Professional Hygiene products and solutions.

Essity´s vision is: Dedicated to improving well-being through leading hygiene and health solutions. BSN medical has joined forces with the Incontinence Care unit, creating the business unit Health & Medical Solutions (HMS), led by Margareta Lehmann. HMS is aligned under one vision - to empower customers, patients and caregivers with products and solutions to support healthy and active lives.

• Production Capacity: 100000

Simple. Safe. Effective.

Arista AH is a 100% plant based absorbable surgical hemostatic powder derived from purified plant starch. The power of Arista AH lies in its Microporous Polysaccharide Hemospheres, a patented blood clotting technology.

Arista AH is indicated in surgical procedures (except neurologic and ophthalmic) as an adjunctive hemostatic device to assist when control of capillary, venous, and arteriolar bleeding by pressure, ligature, and other conventional procedures are ineffective or impractical.

1 Arista AH PMA P050038 Clinical Study.
2 See full Instructions for Use for detailed application instructions.
3 Arista AH Instructions for Use.

INDICATIONS

Arista AH is indicated in surgical procedures (except neurological and ophthalmic) as an adjunctive hemostatic device to assist when control of capillary, venous, and arteriolar bleeding by pressure, ligature, and other conventional procedures are ineffective or impractical.

CONTRAINDICATIONS

Do not inject or place Arista AH into blood vessels as potential for embolization and death may exist.

WARNINGS

Arista AH is not intended as a substitute for meticulous surgical technique and the proper application of ligatures or other conventional procedures for hemostasis.

Once hemostasis is achieved, excess Arista AH should be removed from the site of application by irrigation and aspiration particularly when used in and around foramina of bone, areas of bony confine, the spinal cord, and/or the optic nerve and chiasm. Arista AH swells to its maximum volume immediately upon contact with blood or other fluids. Dry, white AristaAH should be removed. The possibility of the product interfering with normal function and/or causing compression necrosis of surrounding tissues due to swelling is reduced by removal of excess dry material.

Safety and effectiveness of Arista AH have not been clinically evaluated in children and pregnant women. Because there have been reports of decreased amylase activity in newborns up to 10 months, absorption rates of Arista AH in this population may be longer than 48 hours.

Arista AH should be used with caution in the presence of infection or in contaminated areas of the body. If signs of infection or abscess develop where Arista AH has been applied, re-operation may be necessary in order to allow drainage.

Safety and effectiveness in neurosurgical and ophthalmic procedures has not been established.

Arista AH should not be used for controlling post-partum bleeding or menorrhagia.

PRECAUTIONS

When Arista AH is used in conjunction with autologous blood salvage circuits, carefully follow instructions in the Administration section of the IFU regarding proper filtration and cell washing.

Arista AH is intended to be used in a dry state. Contact with saline or antibiotic solutions prior to achieving hemostasis will result in loss of hemostatic potential.

Arista AH is not recommended for the primary treatment of coagulation disorders.

No testing has been performed on the use of AristaAH on bone surfaces to which prosthetic materials are to be attached with adhesives and is therefore not recommended.

Arista AH is supplied as a sterile product and cannot be resterilized. Unused, open containers of Arista AH should be discarded.

Do not apply more than 50g of Arista AH in diabetic patients as it has been calculated that amounts in excess of 50g could affect the glucose load.

In urological procedures, Arista AH should not be left in the renal pelvis or ureters to eliminate the potential foci for calculus formation. 

• Item Code: SM0005
• Production Capacity: 5000
• Delivery Time: Within 21 Days
• Packaging Details: Export worth Packing

• Simple to use and can be moulded directly around the stoma
• Protects the delicate peristomal skin from the effluents
• Absorbs moisture allowing the area around the ostomy to remain dry
• Protect the adhesive plate and extends wear life by minimizing the risk of leakage
• Remains soft & flexible

• Item Code: 30069100
• Production Capacity: 1000
• Delivery Time: one week
• Packaging Details: 60gm