In this Act, unless the context otherwise requires,-
(
a) "appointed day" means the date on which the provisions of this Act shall come into
force under sub-section (
2) of section;
(b) "Chief Executive Officer" means the Chief Executive Officer of the Procurement
Authority established under this Act;
(
c) "medical consumables" includes gloves, syringes, bandages, cotton wool, sutures,
catheters, tubes, infusion sets, I.V. cannulas, etc., laboratory supplies including pipettes, blood
collecting tubes and microscope supplies and surgical instruments such as scalpels, forceps,
lancets, scissors, etc.;
(
d) "medical device" means any instrument, apparatus, implement, machine, appliance,
implant, reagent for use, software, material or other similar or related article, intended by the
manufacturer to be used, alone or in combination, for human beings, for one or more of the
specific medical purpose of,-
(
i) diagnosis, prevention, monitoring, treatment or alleviation of disease,
(
ii) diagnosis, monitoring, treatment, alleviation of or healing of an injury,
(
iii) investigation, replacement, modification or support of the anatomy or of a
physiological process,
(
iv) supporting or sustaining life,
(
v) control of conception,
(
vi) disinfection of medical devices,
(
vii) providing information by means of examination of specimens derived from the
human body,
and does not achieve its primary intended action by pharmacological, immunological
or metabolic means, in or on the human body, but which may be assisted in its intended
function by such means;
(
e) "medical equipment" means the medical devices requiring calibration, maintenance,
repair, user training and decommissioning - activities (usually managed by clinical or biomedical
engineers) used for the specific purposes of diagnosis and treatment of disease or rehabilitation
following disease or injury of human beings and can be used either alone or in combination with
any accessory, consumable or other piece of medical device or medical equipment but excludes
implantable, disposable or single-use medical devices;
(
f) "medical goods" means medicines, medical consumables, medical devices, medical
equipments or execution of turnkey projects therefor; and includes any other medical goods as the
State Government may, from time to time, in consultation with Procurement Authority, by
notification in the
Official Gazette, specify, to be the medical goods for the purposes of this Act;
(
g) "prescribed" means prescribed by rules made under this Act;
(
h) "procure" or "procurement" means the process of purchase, storage or supply of the
medical goods;
(
i) "Procurement Authority" means the Maharashtra Medical Goods Procurement Authority
established under sub-section (
1) of section 3;
(
j) "regulations" means the regulations made under this Act;
(
k) "rules" means the rules made under this Act;
(
l) "Secretary" means Additional Chief Secretary or Principal Secretary or Secretary of any
administrative Department of the State Government.