| Primary Device ID | 10858901006211 |
| NIH Device Record Key | 24268f7d-8177-4914-8f25-a9e2bd59e1ec |
| Commercial Distribution Discontinuation | 2020-09-18 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | SPY PAQ® |
| Version Model Number | SK6000 |
| Company DUNS | 243730939 |
| Company Name | Novadaq Technologies Inc |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 10858901006211 [Primary] |
| GS1 | 20858901006218 [Package] Package: PAQ [6 Units] Discontinued: 2020-09-18 Not in Commercial Distribution |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-10-16 |
| Device Publish Date | 2016-09-23 |
| 10858901006211 | SK6000 |
| 20858701006265 | LC3006 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SPY PAQ 78699583 3180018 Live/Registered |
Novadaq Technologies Inc. 2005-08-24 |