Primary Device ID | 04953170355929 |
NIH Device Record Key | 350fd53a-571e-49c8-b429-693edf2e0e41 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Olympus |
Version Model Number | MAJ-1444 |
Company DUNS | 711789789 |
Company Name | OLYMPUS MEDICAL SYSTEMS CORP. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx | |
Phone | +1(800)401-1086 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04953170355929 [Primary] |
NWB | Endoscope, accessories, narrow band spectrum |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
[04953170355929]
High-level Disinfectant;Ethylene Oxide;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-10-08 |
Device Publish Date | 2016-09-21 |
14953170409681 | THUNDERBEAT 5 mm,45 cm,Front-actuated Grip Type S |
14953170409674 | THUNDERBEAT 5 mm,35 cm,Front-actuated Grip Type S |
14953170408295 | Single Use Biopsy Forceps FB-245U |
14953170408288 | Single Use Biopsy Forceps FB-235U |
14953170408271 | Single Use Biopsy Forceps FB-225U |
14953170408264 | Single Use Biopsy Forceps FB-215U |
14953170402644 | Single Use Aspiration Needle NA-U201H |
14953170402620 | Single Use Aspiration Needle NA-U201H |
14953170402606 | Single Use Aspiration Needle NA-U201H |
14953170402583 | Single Use Aspiration Needle NA-U201H |
14953170402569 | Single Use Aspiration Needle NA-U201H |
14953170402545 | Single Use Aspiration Needle NA-U201H |
04953170402456 | OLYMPUS ENF-V4 |
04953170402425 | OLYMPUS ENF-VH2 |
14953170401074 | Single Use Surgical Scissors FS-200 |
14953170401050 | Single Use Loop Cutter FS-410 |
14953170401036 | Single Use Loop Cutter FS-410 |
14953170399531 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399524 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399517 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399500 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399494 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399487 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399470 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399463 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399456 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399449 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399432 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399425 | Single Use Preloaded Sphincterotome V(Distal Wireguided) |
14953170399418 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399401 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399395 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399388 | Single Use Preloaded Sphincterotome V (Distal Wireguided) |
14953170399371 | Single Use Sphincterotome V |
14953170399364 | Single Use Sphincterotome V |
14953170399357 | Single Use Sphincterotome V (Distal Wireguided) |
14953170399340 | Single Use Sphincterotome V(Distal Wireguided) |
14953170399333 | Single Use Sphincterotome V(Distal Wireguided) |
14953170399326 | Single Use Sphincterotome V(Distal Wireguided) |
14953170399319 | Single Use Sphincterotome V(Distal Wireguided) |
14953170399302 | Single Use Sphincterotome V(Distal Wireguided) |
14953170399296 | Single Use Sphincterotome V(Distal Wireguided) |
04953170399282 | RHINO-LARYNGO FIBERSCOPE ENF-GP2 |
14953170392235 | THUNDERBEAT 5mm, 20cm, Front-actuated Grip Type X |
14953170392228 | THUNDERBEAT 5mm, 20cm, Front-actuated Grip Type X |
14953170392204 | THUNDERBEAT 5mm, 35cm, Front-actuated Grip Type X |
14953170392198 | THUNDERBEAT 5mm, 35cm, Front-actuated Grip Type X |
14953170392174 | THUNDERBEAT 5mm, 45cm, Front-actuated Grip Type X |
14953170392167 | THUNDERBEAT 5mm, 45cm, Front-actuated Grip Type X |
04953170391965 | INTERFACE FOR OLYMPUS LINK DEVICE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OLYMPUS 98323171 not registered Live/Pending |
OLYMPUS LLC 2023-12-20 |
OLYMPUS 98183718 not registered Live/Pending |
Cable Tie Express LLC 2023-09-17 |
OLYMPUS 98013060 not registered Live/Pending |
Olympuss Sports & Entertainment Group, LLC 2023-05-25 |
OLYMPUS 98002376 not registered Live/Pending |
SSG International, LLC 2023-05-18 |
OLYMPUS 97720732 not registered Live/Pending |
Valmont Industries, Inc. 2022-12-16 |
OLYMPUS 97617017 not registered Live/Pending |
Merino, Michael 2022-10-03 |
OLYMPUS 97493838 not registered Live/Pending |
Track Barn, LLC 2022-07-07 |
OLYMPUS 97493792 not registered Live/Pending |
Track Barn, LLC 2022-07-07 |
OLYMPUS 97234548 not registered Live/Pending |
Icon Technology, Inc. 2022-01-24 |
OLYMPUS 97058514 not registered Live/Pending |
Simple Tire LLC 2021-10-04 |
OLYMPUS 90793668 not registered Live/Pending |
Simple Tire LLC 2021-06-24 |
OLYMPUS 90747738 not registered Live/Pending |
OLYMPUS CORPORATION 2021-06-01 |