MD-NECK

MD-NECK is an injectable class III medical device:
- Treatment can be combined with other therapies.
- It improves the movement of the cervical spine segment and reduces the associated pain.
- It counteracts physiological or pathological deterioration of the joints and tissues involved.
- It can be combined with other treatments.

- GUNA S.P.A.
- NAME: MD-NECK
- COMPOSITION: Collagen of porcine origin, Silicic acid, Sodium chloride, Water for injection.
- PRESENTATION: 10 x 2ml.
- INDICATIONS: Improves mobility of the cervical spine.
- INJECTION DEPTH:
Peri-articular: 26G x 13 mm needle; intra-muscular at trigger points:
26G x 13 mm needle.
Note: Carry out thorough skin disinfection with iodopovidone or chlorhexidine.
Peri-articular route: introduce the needle close to the joint at a depth of 4-13 mm.
Intra-muscularly: introduce the needle into the trigger points at a depth of 4-6 mm.
- PROTOCOL: Peri-articular administration: 1-2 infiltrations per week for 3-5
weeks. Results are already evident from the third week but, depending on the patient's clinical situation, treatment can be continued up to the tenth week without risk.
Intra-muscular administration (trigger points): 1-2 infiltrations per week for 3-5 weeks. Results already evident from the third week but, depending on the patient's clinical situation, treatment can be continued up to the tenth week without risk.
- USE: Strict medical use.

- Vials: 10 x 2ml.

Cervical section of the spine.

Collagen of porcine origin, Silicic acid, Sodium chloride, Water for injection.

- The product should only be injected by trained operators, in a suitable environment, using aseptic technique.
- Injection test in patients with suspected hypersensitivity: if there is a history of allergic reactions, a preliminary intradermal/injective test and observation of the patient for at least 1 hour is recommended.
- Avoid immediate exercise/prolonged mobilisation of the treated area unless indicated.
- Do not extend treatment beyond 10 weeks unless clinically assessed; follow protocols indicated by the manufacturer.
- Do not use after the expiry date; use immediately after opening; do not use if the bottle is damaged.

MD-NECK is contraindicated in the following cases:
- Known hypersensitivity to components (e.g. collagen of porcine origin or other excipients).
- Septic processes or active local/articular infections: do not inject into infected areas or in the presence of an ongoing joint infection.

Counteracts physiological or pathological deterioration of joints and tissues involved in:
- Cervicalgia:
- of muscular and/or nervous origin
- from ageing phenomena
- from postural defects
- by concomitant chronic diseases
- from trauma and injuries.