Primary Device ID | 04713072961532 |
NIH Device Record Key | 1167453c-3bcd-4e4c-8ee4-d68b5255fd77 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FREERIDER |
Version Model Number | LUGGIE ELITE PLUS 3W |
Company DUNS | 658109124 |
Company Name | FREERIDER CORP. |
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 | true |
Device Combination Product | false |
Single Use | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04713072961532 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-29 |
Device Publish Date | 2019-04-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FREERIDER 88602889 not registered Live/Pending |
Rohde & Schwarz SwissQual AG 2019-09-03 |
FREERIDER 87187074 5199230 Live/Registered |
ADIDAS AG 2016-09-29 |
FREERIDER 85009103 not registered Dead/Abandoned |
Sunbeam Products, Inc. 2010-04-08 |
FREERIDER 85009100 3979296 Dead/Cancelled |
Sunbeam Products, Inc. 2010-04-08 |
FREERIDER 77929214 3844959 Dead/Cancelled |
Brooklyn Workshop, Inc. 2010-02-05 |
FREERIDER 77037279 3281966 Live/Registered |
FREERIDER CORP. 2006-11-06 |
FREERIDER 75690041 not registered Dead/Abandoned |
FreeRider.net, Inc. 1999-05-17 |
FREERIDER 75052591 2028833 Dead/Cancelled |
FREERIDER CORPORATION LTD. 1996-02-02 |
FREERIDER 73442698 1301831 Dead/Cancelled |
AMF Incorporated 1983-09-06 |
FREERIDER 73430142 1341041 Dead/Cancelled |
AMF Incorporated 1983-06-13 |