Alginate Dressing with 510k CE for Venous Diabeic Pressure Ulcer

Material: Alginate
Feature: Disposable
Certification: CE, FDA, ISO13485
Ethylene Oxide Sterilization: Radiation
Application: Hospital
Group: All
Customization:
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Rating: 5.0/5
Manufacturer/Factory, Group Corporation

Basic Info.

Model NO.
FD1001
Logo Printing
Both Ok
Silver Alginate
Silver Particle
FDA 510k
Antibacterial
Calcium
Silver Dressing
Heavily Exuding
Venous/ Arterial Leg Ulcer
Diabetic Ulcer
Pressure Ulcer
Donor Sites
Lacerations
Post Surgical Wounds
Moderately Exuding
Transport Package
Aluminum Foil Bag, Paper/Poly Bag
Specification
10 pcs per package
Trademark
LUOFUCON
Origin
Huizhou, Guangdong, China
HS Code
3005901000
Production Capacity
1, 000, 000 PCS/Year

Product Description


Description
LUOFUCON® CMC/silver calcium alginate dressing.
We suppliy:
Silver/CMC alginate dressing, calcium alginate swab hydrocolloid adhesive tap, wound care adhesive dressing, vaseline dressing, paraffin dressing, etc.

LUOFUCON® Alginate Dressing is a sterile disposable soft nonwoven alginate dressing derived from seaweed. In contact with wound exudates, the calcium ion in alginate fibers exchanges with the sodium ion in the exudates, which makes the alginate swell and become gelatinous. The gel creates a moist wound environment. The alginate gel does not adhere to the wound when the dressing changing. This in turn supports the natural healing process.

LUOFUCON® Alginate Dressing (Adhesive) is an alginate dressing with a transparent adhesive film. The adhesive alginate dressing has the same action mechanism as the non-adhesive alginate dressing.

LUOFUCON® Alginate Dressing (Rope) is a soft and non-woven fibre with high absorptivity. The rope is used to fill cavity wound.

Features
Highly absorbent
Non-adherent, avoid eschar and reduce scar
Soft and pliable
Comfortable and easy to use
Moist environment, accelerate wound healing

Indication
The products are indicated for moderately to heavily exuding wounds, cavity wounds and other wounds such as venous/arterial leg ulcer, diabetic ulcer, pressure ulcer, donor sites, abrasions, lacerations and post-surgical wounds.


Suggested Applications:
Pressure, arterial, neuropathic(diabetic) and venous leg ulcers
Surgical wounds
Trauma wounds
Superficial partial thickness burns
Abrasions
Donor sites

Specification:

Brand Name
LUOFUCON

Dressing Type
Silver

Thickness
Normal:5mm,Slim:3mm

Size
Customizable

Latex
No

Function
Highly absorbent
Wound Care Condition Type Abrasions, Donor Sites, Laceration, Neuropathic Ulcers, Open Surgical Wounds, Superficial Partial Thickness Burns, Venous Leg Ulcer


Contraindication
If redness or allergic symptoms appears, please stop using the dressing. And do not use the dressing to dry wound.

Precautions
Do not use if the package is damaged.
It is a disposable product. Do not reuse.
External use only.
For severe physical hypertensive patients, consult the physicians before use.

Instructions for use
Cleanse the wound base with normal saline.
Choose suitable LUOFUCON® Alginate dressing according to the wound area, the dressing should be larger than wound area.
If select the non-adhesive alginate dressing, cut or fold the dressing to fit the wound. Apply directly to wound base. If apply to cavity wound, fill the rope into the wound site. Secure the dressing with second dressing such as tape or wrap.
If choose the adhesive alginate dressing, strip the release liner off the dressing and apply to the wound. Then strip off the backing film.

Removal
The dressing should be changed once it is fully turned into gels. The dressing should not be left in place for longer than seven days. Remove the dressing with forceps or gloved fingers.

Sterilization
All of the LUOFUCON® Alginate products are sterilized by ethylene oxide or radiation.

Package
Separate sealed into the paper-plastic bags, in folding box; Transport carton, sealed with adhesive tapes.

Storage
Store it in a dry and cool place avoiding light.

Regulatory Status
LUOFUCON® Alginate Dressing carries the CE mark according to the directive 93/42/EEC for medical device.

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