ETONOGESTREL implant 1 x 68mg, with applicator s.u.

STD DINJETON6I-

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Former Code(s): -X -

The product is supplied (and stored) sterile, it must remain sterile until its use. Sterile = state of being free from all living microorganisms.
Classification of the medicines in groups and subgroups according to their therapeutic use. The classification used by MSF is based on the WHO Model List of Essential Medicines.
G03AC08
Anatomical Therapeutic Chemical Classification according to WHOCC
Thermosensitive codes are defined for storage and transportation temperature requirements of the products.

OC subscriptions: included in supply or field order tools (e.g. UniField)
SC subscriptions: included in supply or field tools
OC validations: approved for procurement and use by an OC for international or local orders specifying context and activity in Medical Standard Lists (MSL)

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ETONOGESTREL implant

Full Name

Nexplanon®

Therapeutic Action

Progestogen contraceptive for subdermal insertion

Indications

Long-acting contraception, for a maximum of 3 years, after which the implant must be changed.

Instructions for use

Implant consists of a single, flexible, non-biodegradable rod, x-ray detectable.

Each rod is 40 mm in length and 2 mm in diameter, and contains 68 mg of etonogestrel.

Insert subdermally (subcutaneously) on the inner side of the non-dominant upper arm, 8-10 cm from the elbow's bony prominence and 3-5 cm below the biceps, using aseptic technique and local anaesthesia.

Equipment required for insertion

For insertion or removal procedures, follow the manufacturer's instructions.

The implant is supplied in a sterile single-use applicator (rather than a trocar).

Therapeutic alternative: levonorgestrel implant (duration of action: 5 years).

Storage

Below 25°C - Protect from sunlight