Primary Device ID | 05705244003835 |
NIH Device Record Key | 43c71e39-29e8-40ba-bb61-f75163db3711 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | neria™soft 90 cannula |
Version Model Number | 722000-5226 |
Company DUNS | 306032491 |
Company Name | Unomedical A/S |
Device Count | 10 |
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 | false |
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 |
Depth | 6 Millimeter |
Angle | 90 degree |
Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05705244003835 [Primary] |
GS1 | 05705244003842 [Package] Package: Outer box [100 Units] In Commercial Distribution |
GS1 | 05705244010314 [Unit of Use] |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-15 |
05705244003866 | Single use infusion cannula for subcutaneous infusion. The infusion cannula must be used as desc |
05705244003835 | Single use infusion cannula for subcutaneous infusion. The infusion cannula must be used as desc |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NERIA 79063901 3771683 Live/Registered |
Unomedical A/S 2008-11-28 |