| Primary Device ID | 10816513024573 |
| NIH Device Record Key | aa49cb94-39c6-4f31-a2a6-68c0b18726d9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dispenser, Liquid Medication |
| Version Model Number | UA15-415-10-BOT-15BRW |
| Company DUNS | 079636164 |
| Company Name | MPS MEDICAL, 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 | 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816513024576 [Primary] |
| GS1 | 10816513024573 [Package] Contains: 00816513024576 Package: BAG [10 Units] In Commercial Distribution |
| KYX | Dispenser, Liquid Medication |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-12-31 |
| Device Publish Date | 2020-12-23 |
| 10816513023422 - Set, I.V. Fluid Transfer | 2021-01-14 |
| 10816513024573 - Dispenser, Liquid Medication | 2020-12-31 |
| 10816513024573 - Dispenser, Liquid Medication | 2020-12-31 |
| 10816513025174 - Set, I.V. Fluid Transfer | 2020-12-31 |
| 10816513025044 - Set, Administration, Intravascular | 2020-04-21 |
| 10816513025037 - Set, I.V. Fluid Transfer | 2020-04-16 |
| 10816513024993 - Set, Administration, Intravascular | 2020-03-09 |
| 10816513025006 - Set, Administration, Intravascular | 2020-03-09 |
| 10816513025013 - Set, I.V. Fluid Transfer | 2020-03-09 |