| Primary Device ID | 00810101520556 |
| NIH Device Record Key | 4a95bd89-3872-4851-9478-059c85e7ef47 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Firm Touch |
| Version Model Number | 6540MD/2XL |
| Company DUNS | 082745034 |
| Company Name | Elite Safety Products |
| 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 | 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810101520556 [Primary] |
| FMC | 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 | 2022-12-08 |
| Device Publish Date | 2022-11-30 |
| 00810101520495 | 6040BMD (2XL) |
| 00810007198828 | 6040BMD (S) |
| 00810007198682 | 6040BMD (XL) |
| 00810007198675 | 6040BMD (L) |
| 00810007198668 | 6040BMD (M) |
| 00810101520556 | 6540MD/2XL |
| 00810101520549 | 6540MD/XL |
| 00810101520532 | 6540MD/L |
| 00810101520525 | 6540MD/M |
| 00810101520518 | 6540MD/S |
| 00810007198835 | 6550MD (S) |
| 00810007198712 | 6550MD (XL) |
| 00810007198705 | 6550MD (L) |
| 00810007198699 | 6550MD (M) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FIRM TOUCH 88377461 not registered Live/Pending |
Elite Safety Products, Inc. 2019-04-09 |
![]() FIRM TOUCH 72163519 0766060 Dead/Expired |
AVON PRODUCTS, INC. 1963-02-27 |