MD-LUMBAR

Description
Useful medical device for improving the mobility of the joints of the lumbosacral area of ​​the spine, whose main therapeutic treatment consists of the following functions:
1. Barrier effect.
2. Lubricating activity.
3. Mechanical support in case of continuous drug therapy.
The use of MD-LUMBAR is recommended by qualified medical personnel in private or public healthcare facilities for:
- improves lumbar mobility; - promotes muscle relaxation in the lumbosacral area;
- supports lumbar muscle structures;
- relieves localized pain, pain at rest or caused by movement, and postural defects.

How to use
MD-LUMBAR can be used alone or in combination with other medical devices from the same line, to guarantee personalized treatment according to the individual clinical picture.
In cases where supportive treatment is required for the onset of acute pain, MD-LUMBAR can be combined with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these).
In addition, in cases where tissue matrix support therapy is required or a slowdown of physiological aging is required, MD-LUMBAR can be combined with MD-MATRIX and MD-TISSUE.

Periatric therapeutic protocol :
2 treatments in the first 2 weeks; 1 treatment until symptoms improve (on average 8-10 sessions).

Chronic conditions: continue with 1 treatment per week for a month until symptoms improve, then with 1 treatment per month or – as needed – every 45-50 days.

The application area must be aseptic; insert the needle near the lumbar and lumbosacral joints to a depth of 3-4 mm.
For this use of the medical device, the following materials and accessories are recommended:
• Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol-based solution, sterile gauze, ethyl chloride-based skin spray.
• Needles: sterile 27 G.
• Syringes: 5 or 10 cc, depending on the amount of solution to be injected.

components
Collagen of porcine origin.
Excipients: Witch hazel, NaCl, water for injections.

warnings
Disposable.
No cases of hypersensitivity to MD-LUMBAR have been reported.
Contains porcine collagen. Patients with known hypersensitivity to the component or excipients should first undergo a skin prick test and be observed for one hour.
Low back pain requires differential diagnosis from disc herniations, pain secondary to primary or metastatic tumors, and reflected or referred pain of visceral origin.
Slight redness at the injection site may be caused by the mechanical effect of the needle or a skin reaction.
Application may cause symptoms of burning/pain at the injection sites, which generally disappear within 5-10 minutes after the end of treatment.
Skin cleansing/disinfection is necessary before and after application.
Any pyogenic bacteria could cause an abscess at the injection site.
Keep out of the reach and sight of children.
Do not use after expiration.
Use the product immediately after opening.
Do not use if seal is broken or tampered with.
After opening, the contents of the vial should be injected immediately.
Do not use if packaging is damaged.

Conservation
Store between 2°C and 30°C, away from sunlight and frost.
The expiration date refers to the product in its intact packaging, stored correctly.

Format
Pack of 10 sterile 2 ml vials

Code MD04