Primary Device ID | 10380657511850 |
NIH Device Record Key | f2bf8a6d-8afe-4147-978c-2c1cb4abfb95 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Engauge |
Version Model Number | 8065751185 |
Company DUNS | 008018525 |
Company Name | Alcon Laboratories, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com | |
Phone | +1(800)862-5266 |
web.masterus@alcon.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00380657511853 [Primary] |
GS1 | 10380657511850 [Package] Contains: 00380657511853 Package: Box [12 Units] In Commercial Distribution |
HQC | Unit, phacofragmentation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-24 |
10380657517050 | 25+® Short Endoilluminator |
10380657517012 | 27+® Endoilluminator |
10380657515773 | 25 GA Chandelier |
10380657515766 | 23 GA Pik Endoilluminator |
10380657515728 | 25 GA Pik Endoilluminator |
10380657514868 | 25+® Wide Angle Endoilluminator |
10380657514417 | 25+® Endoilluminator |
10380657511850 | 25 GA Wide Angle Endoilluminator |
10380657511843 | 23 GA Wide Angle Endoilluminator |
10380657510037 | 20 GA Shielded Bullet Pik Endoilluminator |
10380657510020 | 20 GA Pik Endoilluminator |
10380657510013 | 20 GA End Irrg Endoilluminator |
00380657509836 | 20 Ga Straight Illuminated Laser Probe with engauge RFID |
00380657509829 | 20 Ga Curved Illuminated Laser Probe with engauge RFID |
10380657509765 | 25 GA Endoilluminator |
10380657509758 | 20 GA Wide Angle Endoilluminator |
10380657509741 | 20 GA Bullet Endoilluminator |
10380657509734 | 20 GA Shielded Bullet Endoilluminator |
10380657509727 | 23 GA Endoilluminator |
10380657509710 | 20 GA Endoilluminator |