Primary Device ID | 10380657524355 |
NIH Device Record Key | 347cceb2-8a03-4941-ad5f-e323147bcfbd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Constellation, EDGE PLUS, TOTAL PLUS, ULTRAVIT |
Version Model Number | 8065752435 |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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10380657524492 | 23 GA TOTAL PLUS Combined Procedure Pak, Beveled 10,000 CPM ULTRAVIT Probe Wide Angle Endoillumi |
10380657524393 | 27+ TOTAL PLUS Vitrectory Pak, Beveled 10,000 CPM ULTRAVIT Probe Straight Endoilluminator |
10380657524386 | 25+ TOTAL PLUS Vitrectory Pak, Beveled 10,000 CPM ULTRAVIT Probe Wide Angle Endoilluminator |
10380657524379 | 25+ TOTAL PLUS Vitrectory Pak, Beveled 10,000 CPM ULTRAVIT Probe Straight Endoilluminator |
10380657524362 | 23 GA TOTAL PLUS Vitrectory Pak, Beveled 10,000 CPM ULTRAVIT Probe Wide Angle Endoilluminator |
10380657524355 | 23 GA TOTAL PLUS Vitrectory Pak, Beveled 10,000 CPM ULTRAVIT Probe Straight Endoilluminator |