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> DevicePMAs@therightstef
Age_blah
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# proj.
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DevicePMAs@therightstef
P060011_S000
Approval for the c-flex model 570c intraocular lens (iol). The device is indicated for primary implantation for the visual correction of aphakia in adults in whom a cataractous lens has been removed
279 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P840039_S051
Approval to modify the directions for use for all legally marketed iols under the referenced pmas, to indicate the iols for use in adult patients. Previously, the iols were indicated for use in perso
484 Bytes
2020-03-03
11
2
-
DevicePMAs@therightstef
P960036_S006
Approval for a trade name change of the memorylens iol. The device will be marketed under the trade name cv232 sre pre-rolled acrylic intraocular lens and is indicated for primary implantation for th
414 Bytes
2020-03-03
11
4
-
DevicePMAs@therightstef
P090022_S000
Approval for the softec hd posterior chamber intraocular lens (pciol). The device is indicated for the replacement of the human crystalline lens following phacoemulsification cataract removal in adul
273 Bytes
2020-03-03
11
3
-
DevicePMAs@therightstef
P910056_S008
Approval to modify the directions for use for all legally marketed iols under the referenced pmas, to indicate the iols for use in adult patients. Previously, the iols were indicated for use in perso
484 Bytes
2020-03-03
11
2
-
DevicePMAs@therightstef
P980040_S041
Approval for a change in the packaging configuration/ delivery system for the tecnis 1-piece intraocular lens (iol), model zcb00. the new packaging configuration will function as both the primary pack
698 Bytes
2020-03-03
11
0
-
DevicePMAs@therightstef
P090022_S001
Approval for modifications to the optic design of the softec hd lens to introduce bi-spheric optic surfaces and changes to the labeling related to the introduction of the modified lens. The device, a
455 Bytes
2020-03-03
11
4
-
DevicePMAs@therightstef
P910058_S012
Approval to modify the directions for use for all legally marketed iols under the referenced pmas, to indicate the iols for use in adult patients. Previously, the iols were indicated for use in perso
484 Bytes
2020-03-03
11
2
-
DevicePMAs@therightstef
P090022_S011
Approval for modifications to the optic body shape and overalldiameter of your softec hd lens to introduce a lens with an ovoid optic and overall diameter of 12.50 mm and changes to your labeling rela
516 Bytes
2020-03-03
11
4
-
DevicePMAs@therightstef
P990080_S000
Approval for the ceeon(tm) edge foldable ultraviolet light-absorbing posterior chamber intraocular lens - model 911a. This device is indicated for primary implantation for the visual correction of ap
365 Bytes
2020-03-03
11
4
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