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> DevicePMAs@therightstef
Age_blah
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# proj.
# Ann.
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DevicePMAs@therightstef
P970034_S000
Indicated for the visual correction of aphakia in persons 60 years of age or older, who are undergoing extracapsular cataract extraction and primary lens implantation. The intraocular lens is intende
439 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P080004_S013
Approval for the model 731 intraocular lens (iol), which adds acontrolled positive spherical aberration to the optic. the device, as modified, will be marketed under the trade name isert gemetric and
368 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P990013_S000
This device is indicated for the correction of aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by phacoemulsification cataract extraction. The lens is to be im
328 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P060011_S005
Approval for the following modifications of the c-flex aspheric iol model 970c: 1) increase of overall diameter from 12.00 mm to 12.50 mm; 2) increase of optic size from 5.75 mm to 6.00 mm; and 3) an
571 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P930014_S009
Approval for the acrysof natural single piece intraocular lens (model sb30al). The device is indicated for the replacement of the human lens to achieve visual correction of aphakia in adults when ext
331 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P880081_S032
Approval for a change in haptic material, addition of the optiedge and of a modified prolate anterior optic surface to the si20nb lens and labeling claims for reduced postoperative spherical aberratio
650 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P080004_S012
Approval for a packaging configuration change for the isert model pc-60ad intraocular lens (iol). The device, as modified, will be marketed under the trade name isert model 230 and is indicated for p
350 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P060022_S006
Approval for design modifications to model mi60l and use of medicel viscoject 2.2 lp60430 inserter with model ao60 and is indicated for the replacement of the human crystalline lens in the visual corr
218 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P930014_S000
Approval for the ACRYSOf Models MA60BM and MA30BA Ultraviolet-Absorbing Acrylic Foldable UV-Absorbing Posterior Chamber Intraocular Lenses (IOLs). These devices are indicated for replacement of the h
426 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P990014_S000
This device is indicated for primary implantation for the visual correction of aphakia in patients 60 years of age or older where a cataractous lens has been removed by extracapsular extraction method
259 Bytes
2020-03-03
11
4
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