| Primary Device ID | 00841912100309 |
| NIH Device Record Key | 189bd629-a572-403c-9a79-f6aff5ac85c6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Probe Cover Kit |
| Version Model Number | 2216 |
| Catalog Number | 2216SOM |
| 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841912100309 [Primary] |
| GS1 | 10841912100306 [Package] Package: [24 Units] In Commercial Distribution |
| KKX | Drape, Surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-16 |
| 10841912105677 | 1467 |
| 00841912104949 | 2221 |
| 00841912104574 | 1241 |
| 10841912104274 | 2320 |
| 10841912100757 | 1460 |
| 10841912100740 | 1460 |
| 10841912100733 | 1460 |
| 10841912100726 | 1460 |
| 10841912100719 | 1270 |
| 10841912100702 | 1240 |
| 10841912100696 | 1236 |
| 10841912100573 | 1026 |
| 10841912100474 | 2450 |
| 10841912100467 | 2450 |
| 10841912100450 | 2320 |
| 10841912100443 | 2320 |
| 10841912100436 | 2290 |
| 10841912100429 | 2270 |
| 10841912100412 | 2252 |
| 10841912100405 | 2250 |
| 10841912100399 | 2236 |
| 10841912100351 | 2230 |
| 10841912100320 | 2220 |
| 00841912100316 | 2219 |
| 00841912100309 | 2216 |
| 00841912100293 | 2220 |
| 10841912100252 | 2210 |
| 10841912100245 | 2208 |