Primary Device ID | 10380657531094 |
NIH Device Record Key | c093941f-34ab-42a6-879e-f2df9e3c62c9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CONSTELLATION® HYPERVIT® TOTAL PLUS® |
Version Model Number | 8065753109 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00380657531097 [Primary] |
GS1 | 10380657531094 [Package] Contains: 00380657531097 Package: [6 Units] In Commercial Distribution |
MLZ | Vitrectomy, instrument cutter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-12-21 |
Device Publish Date | 2020-12-11 |
10380658300774 | 25+®Ga HYPERVIT® Bevel 20K CPM Wide TOTAL PLUS® Vitrectomy Pak |
10380657531094 | 27+®Ga HYPERVIT® Bevel 20K CPM TOTAL PLUS® Vitrectomy Pak |
10380657531063 | 25+®Ga HYPERVIT® Bevel 20K CPM TOTAL PLUS® Vitrectomy Pak |
10380650000962 | 27+®Ga HYPERVIT® Bevel 20K CPM TOTAL PLUS® Combined Procedure Pak |
10380650000955 | 25+®Ga HYPERVIT® Bevel 20K CPM TOTAL PLUS® Combined Procedure Pak |