Primary Device ID | 07613327303605 |
NIH Device Record Key | af82f398-84e4-4b15-86fe-2836c33239b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Switchpoint Infinity |
Version Model Number | 0678001400 |
Catalog Number | 0678-001-400 |
Company DUNS | 078807493 |
Company Name | STRYKER COMMUNICATIONS 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 | false |
Lot Batch | false |
Serial Number | true |
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 |
Phone | +1(866)726-3705 |
SCC-CS2@stryker.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327303605 [Primary] |
OCS | Endoscopic video imaging system/component, gastroenterology-urology |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-07 |
07613327054507 - FLEXIS | 2023-06-15 |
07613327589344 - OPERON | 2022-03-30 Pad Set 20" Leg, W Cutout, 3" |
07613327054286 - NA | 2020-08-06 Suspension, Navigation System, 10' |
07613327054293 - NA | 2020-08-06 Suspension, Navigation System |
07613327054514 - NA | 2020-08-06 Medium-Duty Dual Yoke |
07613327054521 - NA | 2020-08-06 Medium-Duty Suspension |
07613327054538 - NA | 2020-08-06 Light-Duty Suspension |
07613327166712 - NA | 2020-08-06 Suspension, Single Universal Flat Panel, Ceiling, 10' |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SWITCHPOINT INFINITY 78294029 2946768 Live/Registered |
STRYKER CORPORATION 2003-08-29 |