| Primary Device ID | 10076490726109 |
| NIH Device Record Key | 224e4f8d-df7f-493e-9a37-c272e24b4b01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KIMTECH |
| Version Model Number | 53137 |
| Catalog Number | 53137 |
| Company DUNS | 111267330 |
| Company Name | Ansell Healthcare Product |
| Device Count | 2 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.com | |
| Phone | 775-470-7106 |
| don.cronk@ansell.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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00076490738501 [Unit of Use] |
| GS1 | 10076490726109 [Primary] |
| GS1 | 20076490738918 [Package] Package: Case [10 Units] In Commercial Distribution |
| LZC | Medical Glove, Specialty |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-09 |
| Device Publish Date | 2025-07-01 |
| 10076490726109 | KIMTECH STERLING NITRILE-XTRA (XS), POWDER-FREE EXAM GLOVES |
| 20076490756707 | KIMTECH STERLING NITRILE-XTRA (XL), POWDER-FREE EXAM GLOVES |
| 20076490753089 | KIMTECH STERLING NITRILE-XTRA (S), POWDER-FREE EXAM GLOVES |
| 20076490730158 | KIMTECH STERLING NITRILE-XTRA (L), POWDER-FREE EXAM GLOVES |
| 20076490723617 | KIMTECH STERLING NITRILE-XTRA (M), POWDER-FREE EXAM GLOVES |
| 20076490768878 | KIMTECH STERLING NITRILE (XS) POWDER-FREE EXAM GLOVES |
| 20076490763743 | KIMTECH PURPLE NITRILE-XTRA (XS) POWDER-FREE EXAM GLOVES |
| 20076490763101 | KIMTECH STERLING NITRILE (L) POWDER-FREE EXAM GLOVES |
| 20076490756875 | KIMTECH PURPLE NITRILE-XTRA (M) POWDER-FREE EXAM GLOVES |
| 20076490755069 | KIMTECH STERLING NITRILE (M) POWDER-FREE EXAM GLOVES |
| 20076490754888 | KIMTECH STERLING NITRILE (S) POWDER-FREE EXAM GLOVES |
| 20076490750262 | KIMTECH PURPLE NITRILE-XTRA (L) POWDER-FREE EXAM GLOVES |
| 20076490748658 | KIMTECH PURPLE NITRILE-XTRA (XL) POWDER-FREE EXAM GLOVES |
| 20076490730592 | KIMTECH STERLING NITRILE (XL) POWDER-FREE EXAM GLOVES |
| 20076490724171 | KIMTECH PURPLE NITRILE-XTRA (S) POWDER-FREE EXAM GLOVES |
| 20076490750088 | KIMTECH POLARIS - XTRA (M) NITRILE POWDER-FREE EXAM GLOVES |
| 20076490736495 | KIMTECH POLARIS - XTRA (L) NITRILE POWDER-FREE EXAM GLOVES |
| 20076490729312 | KIMTECH POLARIS - XTRA (XL) NITRILE POWDER-FREE EXAM GLOVES |
| 20076490727141 | KIMTECH POLARIS - XTRA (S) NITRILE POWDER-FREE EXAM GLOVES |
| 20076490721248 | KIMTECH POLARIS - XTRA (XS) NITRILE POWDER-FREE EXAM GLOVES |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() KIMTECH 98325696 not registered Live/Pending |
Kimberly-Clark Worldwide, Inc. 2023-12-21 |
![]() KIMTECH 88939145 not registered Live/Pending |
Kimberly-Clark Worldwide, Inc. 2020-05-29 |
![]() KIMTECH 86359255 4711849 Live/Registered |
Kimberly-Clark Worldwide, Inc. 2014-08-06 |
![]() KIMTECH 86268329 4613968 Live/Registered |
KIMBERLY-CLARK WORLDWIDE, INC. 2014-05-01 |
![]() KIMTECH 86268326 4613967 Live/Registered |
KIMBERLY-CLARK WORLDWIDE, INC. 2014-05-01 |
![]() KIMTECH 78294911 not registered Dead/Abandoned |
Kimberly-Clark Worldwide, Inc. 2003-09-02 |
![]() KIMTECH 75852116 2562309 Dead/Cancelled |
KIMBERLY-CLARK WORLDWIDE, INC. 1999-11-18 |
![]() KIMTECH 75851897 2553520 Dead/Cancelled |
KIMBERLY-CLARK WORLDWIDE, INC. 1999-11-18 |