| Primary Device ID | 00889024504615 |
| NIH Device Record Key | a756e574-c754-4ba8-afef-028faa2dcb72 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ActiveCare® DVT |
| Version Model Number | A502B000103 |
| Catalog Number | A502B000103 |
| Company DUNS | 137354267 |
| Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024504615 [Primary] |
| JOW | SLEEVE, LIMB, COMPRESSIBLE |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-04 |
| Device Publish Date | 2019-02-01 |
| 00889024504653 | A502B000111 |
| 00889024504646 | A502B000109 |
| 00889024504622 | A502B000105 |
| 00889024504615 | A502B000103 |
| 00889024504530 | A502B000102 |