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

https://medicalguidelines.msf.org/en/node/798
https://unicat.msf.org/cat/product/11681
STD DINJETON6I-

Valid Article

Former Code(s): -
The product is supplied (and stored) sterile, it must remain sterile until its use. Sterile = state of being free from all living microorganisms.
22.1.5 - Implantable contraceptives
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
1525
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

Therapeutic Action

Progestogen contraceptive for subdermal implantation

Indications

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

Instructions for use

Implant composed of one non-biodegradable flexible rod, x-ray detectable.

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

Insert under the skin, on the inside of the non-dominant arm, 8-10 cm from the bony process of the elbow and 3-5 cm below the biceps, under local anaesthetic and aseptically.

Equipment needed for insertion

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

Implant packaged in a sterile single-use applicator (instead of a trocar).

Therapeutic alternative: levonorgestrel implant with a duration of action of 5 years.

Storage

Below 25°C - Protect from sunlight