Primary Device ID | 00785811435769 |
NIH Device Record Key | fb252fd5-80c9-49e0-8af9-318637d66ce5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Boston 7 |
Version Model Number | satafocon A |
Catalog Number | Boston 7 |
Company DUNS | 058816302 |
Company Name | BAUSCH & LOMB INCORPORATED |
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 | false |
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 | 00785811435769 [Primary] |
HQD | Lens, Contact (Other Material) - Daily |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-10-24 |
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10757770618887 - enVista Aspire toric IOL | 2023-11-27 enVista Aspire toric hydrophobic acrylic IOL (non-preloaded) +8.00D SE / +1.50D CYL |
10757770618894 - enVista Aspire toric IOL | 2023-11-27 enVista Aspire toric hydrophobic acrylic IOL (non-preloaded) +8.50D SE / +1.50D CYL |
10757770618900 - enVista Aspire toric IOL | 2023-11-27 enVista Aspire toric hydrophobic acrylic IOL (non-preloaded) +9.00D SE / +1.50D CYL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BOSTON 7 74456621 1960776 Dead/Cancelled |
POLYMER TECHNOLOGY (U.S.A.) CORPORIOHPOLYMER TECHNOLOGY (U.S.A.) CORPORATION 1993-11-05 |
BOSTON 7 74456188 1947301 Dead/Cancelled |
WILMINGTON PARTNERS L.P. 1993-11-05 |