Primary Device ID | 20858701006326 |
NIH Device Record Key | fd5dacea-f85c-42a4-add2-92a125a82153 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SPY-PHI System |
Version Model Number | HH2000 |
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 | 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 | 10858701006329 [Primary] |
GS1 | 20858701006326 [Package] Contains: 10858701006329 Package: Pack [20 Units] In Commercial Distribution |
GS1 | 20858701006333 [Package] Contains: 10858701006329 Package: Pack [48 Units] 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 | 2024-02-29 |
Device Publish Date | 2017-03-31 |
00858701006193 | SPY-PHI Portable Handheld Imaging System |
20858701006289 | SPY-PHI Kit |
20858701006326 | SPY-PHI drape |