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 |