| Primary Device ID | 10884521100152 |
| NIH Device Record Key | f28708d7-b982-46fe-a276-515f96b0a1ac |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A-V Impulse |
| Version Model Number | 6060 |
| Catalog Number | 6060 |
| Company DUNS | 080935429 |
| Company Name | Cardinal Health, 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;Fragile;AVOID DIRECT SUNLIGHT |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521100152 [Primary] |
| JOW | SLEEVE, LIMB, COMPRESSIBLE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 7 |
| Public Version Date | 2019-04-15 |
| Device Publish Date | 2016-10-13 |
| 20884521101453 | Tubing Assembly, Unrestricted, Blue |
| 10884521078123 | Impad Rigid Sole Foot Cover, Large |
| 10884521078116 | Impad Rigid Sole Foot Cover, Medium |
| 10884521077386 | Impad Rigid Sole Foot Cover, X- Large |
| 10884521077379 | Impad Rigid Sole Foot Cover, Large |
| 10884521077348 | Impad Rigid Sole Foot Cover, Medium |
| 10884521077300 | Impad Rigid Sole Foot Cover;Small |
| 10884521100190 | 6000 Series Controller,Refurbished |
| 10884521100152 | 6000 Series Controller |
| 20884521077277 | Impad Rigid Sole Foot Cover,Left |
| 20884521077260 | Impad Rigid Sole Foot Cover,Right |
| 10884521043923 | 6000 Series Controller |