| Primary Device ID | 10787081122926 |
| NIH Device Record Key | 4f01c572-ccda-4cf2-95fb-3803e188e587 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HandArmor |
| Version Model Number | GDNPF102S |
| Catalog Number | GDNPF102S |
| Company DUNS | 007900020 |
| Company Name | TRANZONIC COMPANIES, THE |
| Device Count | 100 |
| 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 | 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 | true |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com | |
| Phone | 8003219832 |
| info@hospeco.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00787081122929 [Primary] |
| GS1 | 10787081122926 [Package] Contains: 00787081122929 Package: box [10 Units] In Commercial Distribution |
| GS1 | 70787081122928 [Unit of Use] |
| LZA | Polymer Patient Examination Glove |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-04-10 |
| Device Publish Date | 2020-04-02 |
| 10787081122957 | NITRILE POWDER FREE EXAM GLOVES BLACK, 10/100-EX-LARGE |
| 10787081122940 | NITRILE POWDER FREE EXAM GLOVES BLACK, 10/100-LARGE |
| 10787081122933 | NITRILE POWDER FREE EXAM GLOVES BLACK, 10/100-MEDIUM |
| 10787081122926 | NITRILE POWDER FREE EXAM GLOVES BLACK, 10/100-SMALL |
| 10787081122360 | NITRILE POWDER FREE EXAM GLOVES BLUE, 10/100-XX-LARGE |
| 10787081122353 | NITRILE POWDER FREE EXAM GLOVES BLUE, 10/100-EX-LARGE |
| 10787081122346 | NITRILE POWDER FREE EXAM GLOVES BLUE, 10/100-LARGE |
| 10787081122339 | NITRILE POWDER FREE EXAM GLOVES BLUE, 10/100-MEDIUM |
| 10787081122322 | NITRILE POWDER FREE EXAM GLOVES BLUE, 10/100-SMALL |
| 10787081114341 | LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, LG |
| 00787081114344 | LATEX HIGH RISK POWDER FREE GLOVES 13 MIL BLUE, 10/50, LG |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HANDARMOR 88855853 not registered Live/Pending |
Robert Kocher 2020-04-01 |
![]() HANDARMOR 85459062 4502130 Live/Registered |
The Tranzonic Companies 2011-10-28 |
![]() HANDARMOR 78102968 2760502 Dead/Cancelled |
STEADYHOLD PRODUCTS, LLC 2002-01-16 |