Primary Device ID | 05705244000476 |
NIH Device Record Key | 4d6571f5-85e2-4513-9b43-db092592b066 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | neria™ |
Version Model Number | 78-060-2736 |
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 | 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 |
Angle | 90 degree |
Angle | 90 degree |
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 | 05705244000476 [Primary] |
GS1 | 05705244000483 [Package] Package: Outer box [200 Units] In Commercial Distribution |
GS1 | 05705244010598 [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 | 3 |
Public Version Date | 2020-03-13 |
Device Publish Date | 2016-09-15 |
05705244004337 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244004191 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244004153 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244004139 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244004054 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003958 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003934 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003750 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003613 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003590 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003491 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244003439 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244001794 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244001770 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244001619 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244001596 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244001572 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244001077 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000759 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000711 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000674 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000636 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000612 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000599 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000575 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000551 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000513 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000476 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000452 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000438 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000292 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000230 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000216 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000193 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000179 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000155 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000131 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
05705244000117 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NERIA 79063901 3771683 Live/Registered |
Unomedical A/S 2008-11-28 |