Primary Device ID | 00785811435691 |
NIH Device Record Key | fa7b66c8-b1f3-4a9a-a95e-c5d9024121d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Boston EO |
Version Model Number | enflufocon B |
Catalog Number | Boston EO |
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 | 00785811435691 [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 |
00757770403417 - Bausch + Lomb | 2024-09-05 HOOK MUSCLE JAMESON |
00757770403660 - Bausch + Lomb | 2024-09-05 PRB LACH 3-4 WILLIAMS |
00757770404933 - Bausch + Lomb | 2024-09-05 HOOK IRIS SHARP TYRELL |
00757770405350 - Bausch + Lomb | 2024-09-05 PROBE STORZ BOWMAN 00 - 0 |
00757770405800 - Bausch + Lomb | 2024-09-05 PRB LACH 1-2 WILLIAMS |
00757770406159 - Bausch + Lomb | 2024-09-05 HOOK IRIS SHARP MAUMENEE |
00757770406364 - Bausch + Lomb | 2024-09-05 SPATULA IRIS CULLER |
00757770407262 - Bausch + Lomb | 2024-09-05 SPATULA CYCLODIALYSIS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BOSTON EO 90849160 not registered Live/Pending |
Bausch & Lomb Incorporated 2021-07-26 |
BOSTON EO 75459821 2336671 Live/Registered |
BAUSCH & LOMB INCORPORATED 1998-03-31 |