| Primary Device ID | 05705244002098 |
| NIH Device Record Key | 7cf83ac9-a793-4876-952c-f1cbe8aa443b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | neria™multi |
| Version Model Number | 721060-2731 |
| 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 |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Device Size Text, specify | 0 |
| Depth | 10 Millimeter |
| Angle | 90 degree |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from direct sunlight. Store at room temperature |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05705244002098 [Primary] |
| GS1 | 05705244002104 [Package] Package: Outer box [120 Units] In Commercial Distribution |
| GS1 | 05705244010192 [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 | 2020-03-18 |
| Device Publish Date | 2016-09-15 |
| 05705244004399 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244004177 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244004078 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244004016 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002210 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002197 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002173 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002159 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002135 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002111 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002098 | Single use infusion set for subcutaneous infusion. The infusion set must be used as described in |
| 05705244002074 | 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 |