| Primary Device ID | 10193494450912 |
| NIH Device Record Key | 1386eab9-20a9-4d07-a995-0eda3160a11a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ON-Q* Pain Relief System |
| Version Model Number | 45091 |
| Catalog Number | PS12504-A-N |
| Company DUNS | 079375431 |
| Company Name | Avanos Medical, Inc. |
| Device Count | 1 |
| 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 | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM | |
| Phone | +1(844)428-2667 |
| PIQ@AVANOS.COM |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Total Volume | 270 Milliliter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00193494450915 [Primary] |
| GS1 | 10193494450912 [Package] Contains: 00193494450915 Package: CS [5 Units] In Commercial Distribution |
| MEB | Pump, infusion, elastomeric |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-06-23 |
| Device Publish Date | 2020-06-08 |
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