| Primary Device ID | 00888118025852 |
| NIH Device Record Key | 3e667320-cd29-4974-ab4c-543f93bdb7eb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NEEDLE |
| Version Model Number | 20-701-15-07 |
| Company DUNS | 826499238 |
| Company Name | KLS-Martin L.P. |
| 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 | 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 |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com | |
| Phone | +1(904)641-7746 |
| KLS-UDI-Info@klsmartin.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00888118025852 [Primary] |
| MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
[00888118025852]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-08-21 |
| Device Publish Date | 2018-09-26 |
| 00888118025975 | 20-847-21-07 |
| 00888118095602 | 20-825-20-07 |
| 00888118064608 | 39-139-21-07 |
| 00888118064592 | 39-137-21-07 |
| 00888118057310 | 36-029-01-07 |
| 00888118025999 | 20-857-20-07 |
| 00888118025968 | 20-744-23-07 |
| 00888118025951 | 20-743-23-07 |
| 00888118025944 | 20-742-23-07 |
| 00888118025937 | 20-741-23-07 |
| 00888118025920 | 20-724-19-07 |
| 00888118025913 | 20-723-19-07 |
| 00888118025906 | 20-722-19-07 |
| 00888118025890 | 20-721-19-07 |
| 00888118025883 | 20-704-15-07 |
| 00888118025876 | 20-703-15-07 |
| 00888118025869 | 20-702-15-07 |
| 00888118025852 | 20-701-15-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEEDLE 98782499 not registered Live/Pending |
Jalic Inc 2024-10-02 |
![]() NEEDLE 97701191 not registered Live/Pending |
Ferrari Importing Company 2022-12-02 |
![]() NEEDLE 97575550 not registered Live/Pending |
Point One USA, LLC 2022-09-01 |
![]() NEEDLE 90545885 not registered Live/Pending |
Needle Music, LLC 2021-02-25 |
![]() NEEDLE 90269977 not registered Live/Pending |
Needle Technologies LLC 2020-10-21 |
![]() NEEDLE 87775778 5698944 Live/Registered |
Ferrari Importing Company 2018-01-30 |
![]() NEEDLE 86773699 not registered Dead/Abandoned |
Lunatech, LLC 2015-09-30 |
![]() NEEDLE 86521022 4909941 Live/Registered |
BATTENFELD TECHNOLOGIES, INC. 2015-02-02 |
![]() NEEDLE 86100951 4547484 Live/Registered |
Needle, Inc. 2013-10-24 |
![]() NEEDLE 80994257 0994257 Dead/Cancelled |
Emerson Electric Co. 0000-00-00 |
![]() NEEDLE 79377175 not registered Live/Pending |
Holger Kiewe genannt König-Berthold 2023-06-16 |
![]() NEEDLE 76361346 2654248 Dead/Cancelled |
MARKET DIRECTIONS, INC. 2002-01-18 |