Primary Device ID | 05705244004078 |
NIH Device Record Key | 91933ea0-3fa6-4e1f-85ba-f7d53dad29d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | neria™multi |
Version Model Number | 721060-2738 |
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 | 05705244004078 [Primary] |
GS1 | 05705244004085 [Package] Package: Outer box [120 Units] In Commercial Distribution |
GS1 | 05705244010215 [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 |