Primary Device ID | 10380657900227 |
NIH Device Record Key | a963f626-8a7e-4ed7-93c6-791b0a5315d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Alcon, TurboSonics, ABS, MicroTip |
Version Model Number | 8065790022 |
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 |
Outer Diameter | 0.9 Millimeter |
Outer Diameter | 0.9 Millimeter |
Angle | 30 degree |
Outer Diameter | 0.9 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00380657900220 [Primary] |
GS1 | 10380657900227 [Package] Contains: 00380657900220 Package: Box [6 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 |
10380657900234 | 45° Kelman®, 0.9 mm TurboSonics® ABS® MicroTip™ Tip |
10380657900227 | 30° Kelman®, 0.9 mm TurboSonics® ABS® MicroTip™ Tip |
10380657900203 | 30° Round, 0.9 mm TurboSonics® ABS® MicroTip™ Tip |