Primary Device ID | 04714379292145 |
NIH Device Record Key | 041e397d-f10c-4a2d-b897-5dd39729ba03 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MERITS |
Version Model Number | P323 30200576 |
Company DUNS | 657231924 |
Company Name | MERITS HEALTH PRODUCTS CO., LTD. |
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 | true |
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 | 04714379292145 [Primary] |
ITI | Wheelchair, 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 | 2018-10-16 |
Device Publish Date | 2018-09-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MERITS 87119600 not registered Dead/Abandoned |
Hollodeck Creations, Inc. 2016-07-28 |
MERITS 78230150 2910415 Dead/Cancelled |
Canadian Imperial Bank of Commerce 2003-03-26 |
MERITS 76250929 2520122 Live/Registered |
Merits Health Products, Inc. 2001-05-03 |
MERITS 75849493 2484501 Live/Registered |
CAMPBELLWILSON, LLP 1999-11-12 |