Primary Device ID | 00785811435677 |
NIH Device Record Key | 30d72a08-8419-4a4c-8f59-092be5042b81 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Boston XO2 |
Version Model Number | hexafocon B |
Catalog Number | Boston XO2 |
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 | 00785811435677 [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 |
00757770407309 - Bausch + Lomb | 2025-01-07 TNMTR STORZ-SCHIOTZ AUTOCLAV |
00757770408856 - Bausch + Lomb | 2025-01-07 TNMTR ALLEN-SCHIOTZ PLNGR RETR |
00757770417629 - Bausch + Lomb | 2025-01-07 X-WGT F/E5754&E5755 5.5 GR |
00757770419944 - Bausch + Lomb | 2025-01-07 LOOP LENS KIRBY |
00757770420803 - Bausch + Lomb | 2025-01-07 X-WGT F/E5754&E5755 7.5 GR |
00757770424399 - Bausch + Lomb | 2025-01-07 KNIFE FOREIGN BODY ELLIS |
00757770426867 - Bausch + Lomb | 2025-01-07 X-WGT F/E5754&E5755 10.0 GR |
00757770433421 - Bausch + Lomb | 2025-01-07 CANNULA BRUSH FOR HANDPIECE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BOSTON XO2 77157610 3489612 Dead/Cancelled |
BAUSCH & LOMB INCORPORATED 2007-04-16 |
BOSTON XO2 77152610 3489577 Live/Registered |
Bausch & Lomb Incorporated 2007-04-10 |