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About Us

SPM MEDICARE PVT. LTD that has set-up a state-of-the-art manufacturing facility in the National Capital Region (NCR) of India for manufacturing Disposable Medical Devices and Disposable Apparel Range.
Since the Company's inception in 2015, SPM Medicare has emerged as one of the fastest growing companies in India in the medical sector, and the Company has won laurels for its commitment to Quality and Service in manufacturing and exporting finest disposable medical products at competitive prices.
We have installed top-of-the-line automatic machines in our medical disposable manufaturing facility with a quest to achieve optimized manufacturing processes and to achieve highly safe and quality products. We manufacture all products under Clean Room Areas, and we have in-house ETO Sterilizer and dedicated Quality Lab equipped to meet national and international regulatory requirements. In addition to this, ease in the availability of raw material, experienced and dedicated team, and backing from leading financial institutions helps us to operate smoothly and reliably. We also value the hygiene and safety of our workers and ensure that they wear recommended safety gear during production.
The Company maintains and follows the Quality Management System as per ISO 13485 certified by TUV Rhineland (Germany). Further our products have also received CE certification from TUV Rheinland (Germany) and UKCert (UK). With above Certifications in place from the most stringent quality authorities, we have been able to Market and place our disposable medical products in more than 20 countries around the world.
We are an organization that follows ethical values and believes in team work and respect for people. We always try to be a step ahead in our Marketing endeavours and believe in regularly adding new products to our portfolio.
Medbits by SPM Medicare
14 MOTHERS AFFLICTED BY SURGICAL SITE INFECTION AT YAVATMAL
Date : 21st Aug. 2019Edition : Vol. 1, Editorial 1
DISPOSABLE vs REUSABLE GOWNS: (A BATTLE FOR INFECTION CONTROL AND SUSTAINABILITY)
Date : 29th Aug. 2019Edition : Vol. 1, Editorial 2
THE PASSAGE OF BACTERIA THROUGH SURGICAL DRAPES.
Date : 11th Sept. 2019Edition : Vol. 1, Editorial 3 The passage of bacteria through surgical drapes is a potential cause of wound infection. Previous studies have shown that liquids and human albumin penetrate certain types of drapes. We studied the passage of bacteria through seven different types of surgical drape and an operating tray. Bacteria easily penetrated all the woven re-usable fabrics within 30 min. The disposable non-woven drapes proved to be impermeable, as did the operating tray. We recommend the use of non-woven disposable drapes or woven drapes with an impermeable operating tray in all surgical cases. Infection remains a problem despite modem aseptic surgical techniques and the routine use of antibiotics. There is also growing concem over the infection of healthcare workers by patients, particularly those with the hepatitis and human immunodeficiency viruses (HIV). It has been postulated that acquired immunodeficiency syndrome (AIDS) can be acquired by skin contact with HIV-infected blood. Braathen et al. suggested that HIV has an affinity for the Langerhans’ cells of the skin9 and, in 1987, the Centers for Disease Control reported three cases of non- percutaneous transmission of HIV in healthcare workers. In the operating theatre, infective organisms can be spread either directly by means of instruments, hands and penetration of drapes and gowns, or indirectly through air contamination. Whyte et al. and Hubble et al. have shown that air contamination, caused by shedding of bacteria by theatre personnel, is a significant cause of wound contamination. They suggested special clothing with occlusive cuffs to prevent shedding. The passage of bacteria through surgical drapes poses a major concern. Mackintosh and Lidwell performed experiments to determine the resistance to penetration by aqueous fluids of certain materials commonly used to make surgical drapes. Untreated woven fabrics are rapidly penetrated; non-woven synthetic materials resisted longer and tightly woven cotton fabrics resisted the longest.Ha’eri and Wlley used human albumin microspheres labelled with Tc as tracer particles to determine the permeability of drapes. The particles penetrated woven drapes, but not non-woven drapes. This study does not take into account the physical and biological differences between albumin and bacteria. These differences may affect rates of penetration. Using a new method to assess the permeability of fabrics, we performed an experiment to determine the passage of Streptococcus viridans and coagulase-negative Staphylococci spp. (common skin commensals) through various wet surgical drapes. Materials and Methods We tested seven types of surgical drapes that are in common use in operating theatres in the Bristol hospitals, as well as a PVC operating tray. Twenty-four round agar plates, with a diameter of 90 mm, were prepared by filling them to the brim with Columbia agar (Becton Dickenson, Oxford, UK) containing 8% whole horse blood (TCS Microbiology). The plates were inoculated with 10 colony forming units of Strep. viridans and coagulase-negative Staphylococcus and incubated in air at 37°C for 18 h. The plates were divided into eight sets of three plates. A set of agar plates was assigned to each type of drape to be tested. A sterile section of drape was placed over each agar plate. Each drape was then wet with 15 ml sterile normal saline placed with a sterile pipette over the centre of each agar plate. Twenty-four square agar plates, 100 mm x 100 mm in size, were filled to the brim with blood agar. Each of these plates was inverted and placed over a round agar plate. After 30, 60 and 90 min, a square agar plate was removed from each set and incubated for 48 h. All the square plates were inspected for growth of Strep. viridans and coagulase-negative Staphylococci spp. The experiment was then repeated a second time to check for reproducibility. Results Scanty growth was defined as less than 10 colonyforming units. Moderate growth was defined as 10-10 colony-forming units. Heavy growth was defined as >10 colony-forming units. All of the reusable woven drapes allowed penetration by bacteria within 30 min. Drapes made of non- woven synthetic materials were impermeable (Tables 1). Abstract : Ann R Coll Surg Engl. (2000 Nov; 82(6): 405–407.) Department of Orthopaedic Surgery, University of Bristol, UKSAFETY OF THE SURGEON: ‘DOUBLE-GLOVING’ DURING SURGICAL PROCEDURES
Date : 20th Sept. 2019Edition : Vol. 1, Editorial 4
GLOVINGPATTERN | PERFORATIONS | NO(%)WITHVISIBLESKINCONTAMINATION |
Single Glove | 19 | 8(42.1) |
Double Glove | 22 | 5(22.7) |
DOUBLE GLOVING : MYTH VERSUS FACT
Myth1 : Needle sticks and sharp injuries are uncommon events. Truth: – Cuts or needle sticks may occur in as many as 15 percent of operations. – Up to 16 percent of injuries occur while passing sharp instruments hand-to-hand. – Suture needles are the most frequent source of injury and are involved in as many as 77 percent of total injuries. Most injuries are self-inflicted, but a notable number, perhaps as many as 24 percent, are inflicted by a co- worker. -Most, if not all, surgeons have encountered blood on their hands or fingers at the conclusion of a procedure without being aware of an injury or glove barrier breach by any other method (glove puncture tear or failure). The practice of wearing two pairs of gloves offers a high degree of protection from this common event. Myth2 : The glove failure rate is equally high with double gloves as with single Truth: – Double-gloving reduces the risk of exposure to patient blood by as much as 87 percent when the outer glove is punctured. Volume of blood on a solid suture needle is reduced by as much as 95 percent when passing through two glove layers, thereby reducing viral load in the event of a contaminated percutaneous injury. – One study conducted a prospective, randomized, trial of 143 procedures involving 284 people and found the glove failure rate (i.e., blood contamination of the fingers) was 51 percent when one glove was worn but only 7 percent with double-gloving. Reference : Personal Protective, Infection Control Today By Linda McNeilly member of the Surgical Products team at Cardinal HealthVision and Mission
- To become the most respected organization in the healthcare sector, touching billion lifes across the globe by providing safe and quality products and services.
- To understand the requirements of our customers in the medical and healthcare sectors.
- To design and manufacture high quality products and services as per customer's requirements.
- To establish an environment wherein we are committed to provide world class care.

Plant & Machineries
Molding Area
Molding Machines manufacture the different plastic parts . This machine has been procured from global leaders in plastics injection molding process.

Infusion therapy
IV Sets are manufactured and assembled in Clean Room of class 10,000 by highly skilled and trained manpower to ensure quality and accuracy in assembly process.Fully Automatic Assembly Lines
Fully-automatic Insulin Syringe Assembly machine has been specially designed in South Korea to achieve accuracy, quality, and speed in assembling.

IV cannula
IV Cannula are assembled in Clean Room of class 10,000 by pneumatic machines of latest technology to provide quality, speed and accuracy in the assembly process.World Class Laboratory
Quality Test Laboratory is equipped with test machines and instruments to ensure rigorous Quality Control through-out the manufacturing process

Medical Disposable apparels
Medical Disposable apparels are manufactured in controlled environment by highly trained individuals using high speed stitching and cutting machines.ETO Sterilizer Machine
ETO Sterilizer Machine has been installed to sterilize the packed finished goods to make it completely safe for use. This machine sterilizes by using Ethylene Oxide (EO) gas.
Management
A team of hard-working enthusiastic people who helped this product come to life.

Mr. Umang MathurDirector
He is an engineer from BITS Pilani. Has more than 10 years of rich technical experience. Prior to venturing in the field of medical devices, he held position of Senior Engineer in Rural Electrification Corporation Ltd., a financial institute under the Ministry of Power, Govt. of India

Mr. Vivek S PandeyDirector
Has more than 25 years of experience in production and operations of various CE-marked sterile medical disposals such as Insulin Syringe, Other Syringes, IV sets, Surgical Blades, etc. He has served as Production Manager in leading manufacturing units. He has experience in working with the latest generation cutting edge plant and equipment with strong focus on cost control. He also has outstanding people management skills ensuring harmonious working of units with large manpower.
Contact Us
Get In Touch
- Address : B-40, Phase-II, Noida, U.P.-201305, India
- +91-8407070718
- info@spmmedicare.com