Products Description
Surgical film dressing rolls are thin-film medical products made of PE or PU materials, usually packaged in roll form for easy processing into finished surgical film dressings. The core function is to form a sterile barrier through physical coverage, and some products enhance infection prevention and control capabilities by adding antibacterial ingredients such as iodine.
Classification of surgical film dressing by usage scenarios
1. Conventional surgical procedures
Applicable scenarios: Conventional surgeries such as thoracic surgery, general surgery require covering the incision and blocking contaminants.
Features: Transparent or iodine-containing surgical film dressings are often used to facilitate observation of the surgical field and reduce the risk of infection.
2. Special surgical procedures
Ocular surgery
Demands: Highly transparent and thin surgical dressing to avoid compressing eye tissues and provide a clear field of vision.
Surgery with high risk of infection
Applicable scenarios: Burn repair, contaminated trauma, or surgery for immunocompromised patients.
Features: Iodine-containing surgical membranes are preferred to achieve long-term antibacterial effects through the slow release of iodine ions.
Puncture point protection
Purpose: Cover puncture points such as arteriovenous puncture and epidural anesthesia to prevent liquid contamination and bacterial infection.
Design: Miniaturized cutting for quick fitting without affecting operation.
Postoperative wound care
Applicable scenarios: Short-term protection of suture wounds, mild abrasions or cuts.
Function: Waterproof and breathable material maintains a moist environment, promotes healing and reduces friction stimulation.
Summary The use scenario of surgical membranes should be selected based on the type of surgery, infection risk and operation requirements.
For example:
Conventional surgery mainly uses transparent waterproof type.
High-risk infection surgery requires iodine-containing antibacterial type.
Radiotherapy or puncture operation emphasizes protective fit.
Preoperative preparation and contraindication screening
Check the integrity of the package
Before use, it is necessary to confirm that the outer packaging of the surgical film is not damaged or contaminated to ensure sterility.
Intraoperative operation specifications
Skin pretreatment
The attached area must be thoroughly disinfected and completely dry to avoid residual disinfectant affecting the viscosity.
Avoid excessive stretching
Avoid violent stretching when applying the film to prevent the film from thinning or rupturing and weakening the barrier function.
Postoperative treatment and monitoring
Timely removal and cleaning
After surgery, the surgical film is removed according to the specifications and the residual colloid is cleaned to reduce skin irritation.
Infection monitoring
Observe whether the film area has abnormalities such as redness, swelling, exudation, etc., and check for infection or allergic reaction in time.
Other information
Standard
ISO13485
Certification
FDA Approved
Protection Function
Cover the incision and block contaminants
Product Material
Hypoallergenic.
The material has excellent ductility.
High transparency facilitates real-time observation of the incision and surrounding tissue status during surgery, improving the accuracy of the operation.
Precautions for use
Storage and Management
Store in a cool and dry environment to avoid high temperature or humidity that may cause the colloid to fail.
Check the expiration date of the product before use. The viscosity and protective properties of expired film materials may decrease.
Appendix: General operating principles
After applying the film, the surgical area must be kept stable to avoid damage to the film due to patient movement or friction during surgery.
Some surgical films are highly transparent, which is convenient for observing the wound surface during surgery, but it must be ensured that it does not affect the surgical field and operation.
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