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Note: 35-008(S) & 35-008NS (NS) are the equivalent Protex®4 replacement for 28-206 (S) & ST 0037 (NS).
Product Details
Size
254(230)cm x 317cm
Units Per Inner
-
Inners Per Carton
-
Carton quantity
12 pcs
Sterile
Sterile
Use
Colour
Blue
More Information
VIDEO
35-008 Protex®4 Caesarean T-Drape
Gynaecological Drapes
Multigate Gynaecological Drapes cover the full range of relevant procedures and are known for their exceptional fluid management and infection control. They are cost effective and reduce the risk of contact with body fluids for clinicians and patients.
Relevant Procedures
- 1244 Other excision procedures on ovary
- 1251 Salpingectomy
- 1258 Other procedures on fallopian tube
- 1259 Examination procedures on uterus
- 1260 Insertion or removal of intrauterine device
- 1263 Destruction procedures on uterus
- 1265 Curettage and evacuation of uterus
- 1266 Excision of lesion of uterus
- 1268 Abdominal hysterectomy
- 1269 Vaginal hysterectomy
- 1275 Destruction procedures on cervix
- 1283 Repair of prolapse of uterus, pelvic floor or enterocele
- 1297 Procedures for reproductive medicine
- 1299 Other procedures on female genital organs
Instructional Videos
Protex®4 - Advanced Drape Protection System
Advanced materials technology that improves drape imperviousness and absorbency to deliver unbeatable patient and surgical team protection.
Protex®4 drapes are made from a pliable yet tough impervious bi-laminate material supported by an additional ultra-reinforcement layer to further boost absorbency if required. They are designed to eliminate bacterial transfer and deliver maximum absorbency and strikethrough prevention.
Intellectual Property rights such as patents, patent applications, registered designs etc. apply to this product group.
For details refer to applications: 201613307, 201712340, 201713600, 201713601, 201713962.
Technical Note: "Single Use" Labelled Products
The symbol above is from ISO 15223. Its definition is “Do not re-use”.
As the standard document notes, this symbol is not intended to mean "single patient use" or "single procedure use”. Items labelled as “Single Use” should be placed in the appropriate waste container once the clinical use of the device has finished on the patient.
Single Use equipment is universally recognised as an effective strategy in the healthcare sector which minimises the risks of cross-infection.
Single Use devices don't have to withstand the rigours of reprocessing and allow the use of different materials and more complex designs. All manufacturers are required to have data to show that a Single Use device will function safely for that one use only. Modern devices are commonly fabricated from synthetic materials. The interaction of these devices with the human body often leaves a biofilm on all the surfaces of the device which may be impossible to decontaminate.
Multigate Medical Products does not supply reprocessing instructions for any of our products labelled as “Single Use”.
As with all sterile items, you need to check the integrity of the packaging before use. If the packaging is damaged in any way it can no longer be considered sterile. Items left over from an opened kit or procedure pack that are not used are considered as contaminated from an infection control perspective.
If you have any questions or would like more information on this topic, please contact your local Multigate Business Development Manager or our Customer Service Department.