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ASPIRATION DEVICE, MVA PLUS (Ipas), 60 ml, autoclavable

https://medicalguidelines.msf.org/en/node/9-5-manual-vacuum-aspiration-mva-51417954.html
https://unicat.msf.org/cat/product/18350
STD SCTDMVAS60A

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Former Code(s): -X
CE marking: declaration that the product meets EU standards for health, safety, and environmental protection. The CE marking indicates that the product may be sold freely in any part of the European Economic Area, regardless of its country of origin.
I
In Europe, medical material that fulfills the definition of a medical device according to the MDR (Medical Device Regulation) is classified into 4 classes
CT30
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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ASPIRATION DEVICE, MVA PLUS (Ipas)

Definition

Manual vacuum suction system for uterine evacuation used for incomplete abortions and abortions up to maximum 12 weeks of amenorrhoea (since the last period).

Can be used in an outpatients' room under local anaesthesia.

Specifications

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Technical specifications

  • BARREL:
    • transparent polypropylene (PP)
    • cylindrical
    • graduated in ml and in ounce (oz.)
    • water-repellent graduations every ml and every ¼ of ounce
    • capacity: 60 cc/ml
    • diameter: 2.5 cm
    • vacuum capacity: 60 to 66 cm Hg
  • COLLAR STOP:
    • polypropylene (PP)
    • flexible half ring located on the top of the barrel
    • ended by 2 small rods which protrude into the barrel and prevent the plunger from dislodging
    • to remove the plunger, the collar stop has to be taken off
  • PLUNGER:
    • polypropylene (PP)
    • length: 17.5 cm
    • device to maintain vacuum (when the suction is complete, 2 lateral parts attached to the top of the central part prevent the plunger from retracting)
  • DOUBLE LOCKING VALVE:
    • polypropylene (PP)
    • 2 valve buttons made of polyetherimide
    • cap to fit the cannula
    • removable valve liner
    • allows a vacuum to be generated in the syringe before the procedure (vacuum is held as long as this valve is closed)
  • Supplied with a silicone tube for lubrication and 1 nitrile rubber O-ring
  • Compatible with EasyGrip® cannulae
  • Non sterile device, autoclavable

Packaging & Labelling

Unit packaging: plastic bag.

To be Ordered Separately

  • Easygrip cannula's of different sizes
  • SCTDMVAS1--: SET OF SPARE ACCESSORIES: the set includes 1 of each of the following non-sterile articles:
    • plunger O-ring
    • collar stop
    • cap
    • 2 ml tube of silicone

Instructions for use

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Maintenance

Read carefully the IFU from the manufacturer.

Disassemble the aspiration device before cleaning

Steam autoclave wrapped in a double layer of paper for 30 minutes at 121ºC with a pressure of 106 kPa.

Before use, reassemble, lubricate and check vacuum capability. The aspirator should be discarded and replaced for any of the following reasons:

  • The cylinder is brittle or cracked or mineral deposits inhibit plunger movement.
  • The valve parts are cracked, bent or broken.
  • The buttons are broken.
  • The plunger arms do not lock.
  • The aspirator no longer holds a vacuum.

Storage

  • Store between 15 and 30°C
  • Protect from sunlight ‐ Protect from humidity

MSF requirements

Compared to the sharp-curettage method of abortion, use of MVA requires less cervical dilatation and is associated with less blood loss, shorter hospital stays and a reduced need for anesthetic drugs.

Vacuum aspiration methods are recommended over sharp curettage by the World Health Organization.

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