| Primary Device ID | 00348783001792 |
| NIH Device Record Key | f60f0b2a-0947-445c-84c4-0fed4266a44a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Knit-Pak+ |
| Version Model Number | 9007560 |
| Company DUNS | 014789663 |
| Company Name | PREMIER DENTAL PRODUCTS COMPANY |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00348783001792 [Primary] |
| MVL | Cord, Retraction |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2024-04-03 |
| Device Publish Date | 2024-01-09 |
| 00348783001853 | Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord Sample Pack, Brown - Size 0 |
| 00348783001846 | Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Orange- Size 2, Length – |
| 00348783001839 | Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Blue - Size 1, Length – |
| 00348783001822 | Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Purple - Size 0, Length †|
| 00348783001815 | Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Brown - Size 00, Length †|
| 00348783001808 | Premier® Knit-Pakâ„¢+ Aluminum Chloride Impregnated Retraction Cord, Green - Size 000, Length â |
| 00348783001792 | Premier® Knit-Pak™+ Aluminum Chloride Impregnated Retraction Cord, Dark Green - Size 000.0, L |