Primary Device ID | 00817573024094 |
NIH Device Record Key | 705e6749-9dbe-425a-91d4-2ed83a91581b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hi-Pull |
Version Model Number | 830-514 |
Company DUNS | 045545589 |
Company Name | LANCER ORTHODONTICS, 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 | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817573024094 [Primary] |
DZB | Headgear, Extraoral, Orthodontic |
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 | 2017-01-15 |
00817573024100 | HI-PULL STRAP BLUE LARGE 5/PK |
00817573024094 | HI-PULL STRAP BLUE MEDIUM 5/PK |
00817573024087 | HI-PULL STRAP BLUE SMALL 5/PK |
00817573024070 | HI-PULL STRIP BLUE EXTRA SMALL 5/PK |
00817573024056 | HI-PULL STRAP BLUE LARGE |
00817573024049 | HI-PULL STRAP BLUE MEDIUM |
00817573024032 | HI-PULL STRAP BLUE SMALL |
00817573024025 | HI-PULL STRAP EQUA-PULL ASRT 5/PK |
00817573024001 | HI-PULL STRAP W/SAFETYMODULE600g 1/PK |
00817573023998 | HIGH PULL CAP COTTON 5/PK |
00817573023981 | HIGH PULL CAP COTTON 5/PK |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HI-PULL 97070434 not registered Live/Pending |
NAGAKI SEIKI CO., LTD. 2021-10-12 |
HI-PULL 79161392 4970886 Live/Registered |
NAGAKI SEIKI CO., LTD. 2014-06-10 |