Primary Device ID | 10688503000108 |
NIH Device Record Key | ff4629ed-2a76-490f-abbb-bc431a69d253 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M-SERIES |
Version Model Number | M2F272-1200-00-NA |
Company DUNS | 245449095 |
Company Name | Savaria Concord Lifts Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10688503000108 [Primary] |
FSA | Lift, Patient, Non-Ac-Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-28 |
Device Publish Date | 2023-07-20 |
10688503000016 | Patient lifter |
10688503000009 | Patient lifter |
10688503000177 | Patient lifter |
10688503000160 | Patient lifter |
10688503000153 | Patient lifter |
10688503000146 | Patient lifter |
10688503000139 | Patient lifter |
10688503000122 | Patient lifter |
10688503000115 | Patient lifter |
10688503000108 | Patient lifter |
10688503000092 | Patient lifter |
10688503000085 | Patient lifter |
10688503000078 | Patient lifter |
10688503000061 | Patient lifter |
10688503000054 | Patient lifter |
10688503000047 | Patient lifter |
10688503000030 | Patient lifter |
10688503000023 | Patient lifter |
10688503000184 | Patient lifter |
10688503000191 | Patient lifter |
10688503000238 | Patient lifter |
10688503000221 | Patient lifter |
10688503000214 | Patient lifter |
10688503000207 | Patient lifter |
10688503000245 | Patient lifter |
10688503000252 | Patient lifter |
10688503000290 | Patient lifter |
10688503000283 | Patient lifter |
10688503000276 | Patient lifter |
10688503000269 | Patient lifter |
10688503000320 | Patient lifter |
10688503000313 | Patient lifter |
10688503000306 | Patient lifter |
10688503000344 | Patient lifter |
10688503000337 | Patient lifter |
10688503000351 | Patient lifter |
10688503000368 | Patient lifter |
10688503000375 | Patient lifter |
10688503000382 | Patient lifter |
10688503000405 | Patient lifter |
10688503000399 | Patient lifter |
10688503000412 | Patient lifter |
10688503000429 | Patient lifter |
10688503000450 | Patient lifter |
10688503000443 | Patient lifter |
10688503000436 | Patient lifter |
10688503000467 | Patient lifter |
10688503000528 | Patient lifter |
10688503000511 | Patient lifter |
10688503000504 | Patient lifter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() M-SERIES 98620044 not registered Live/Pending |
Hanson Lab Solutions, LLC 2024-06-26 |
![]() M-SERIES 98571296 not registered Live/Pending |
Particle Industries, Inc. 2024-05-28 |
![]() M-SERIES 98203571 not registered Live/Pending |
S&S Cycle, Inc. 2023-09-29 |
![]() M-SERIES 97793545 not registered Live/Pending |
Digital Media Vending International LLC 2023-02-14 |
![]() M-SERIES 90210334 not registered Live/Pending |
Smart Label Solutions LLC 2020-09-25 |
![]() M-SERIES 88824972 not registered Live/Pending |
J. Bond & Sons Ltd. 2020-03-06 |
![]() M-SERIES 87258642 5240914 Live/Registered |
Caravan Canopy Int'l, Inc. 2016-12-06 |
![]() M-SERIES 85823650 4846394 Live/Registered |
JST PERFORMANCE, LLC 2013-01-15 |
![]() M-SERIES 85799721 4379528 Live/Registered |
MORRIS YACHTS, LLC 2012-12-11 |
![]() M-SERIES 85447589 4339459 Live/Registered |
ARCONIC INC. 2011-10-14 |
![]() M-SERIES 79164592 not registered Dead/Abandoned |
Arnold & Richter Cine Technik; GmbH & Co. Betriebs KG 2015-03-18 |
![]() M-SERIES 78901393 3297821 Live/Registered |
Golf Galaxy Golfworks, Inc. 2006-06-06 |