| Primary Device ID | 10841912106315 |
| NIH Device Record Key | 4a07af21-3063-460b-975e-01fed7a8eeeb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PullUp Probe Cover Kit |
| Version Model Number | 2044 |
| Catalog Number | 2044 |
| Company DUNS | 965417181 |
| Company Name | PROTEK MEDICAL PRODUCTS, 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 | 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 | 00841912106318 [Primary] |
| GS1 | 10841912106315 [Package] Contains: 00841912106318 Package: [24 Units] In Commercial Distribution |
| KKX | Drape, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-14 |
| Device Publish Date | 2020-12-04 |
| 10841912105653 | 2211 |
| 10841912105363 | 2295 |
| 00841912104475 | 2097 |
| 10841912104359 | 1512 |
| 10841912102867 | 2231 |
| 10841912102874 | 2231 |
| 10841912100627 | 1096 |
| 10841912100382 | 2233 |
| 10841912100375 | 2233 |
| 10841912100368 | 2231 |
| 10841912100207 | 2099 |
| 00841912100194 | 2099 |
| 00841912100187 | 2097 |
| 10841912100177 | 2097 |
| 00841912100163 | 2097 |
| 10841912100153 | 2096 |
| 00841912100149 | 2095 |
| 10841912106735 | 2048 |
| 10841912106315 | 2044 |