| Primary Device ID | 00857910006802 |
| NIH Device Record Key | 36d7f563-ab73-4f73-a014-a0d80b6cddf8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RE-CUR ALP® |
| Version Model Number | RE-CUR ALP® 4 THIGH-L |
| Catalog Number | 500008R |
| Company DUNS | 079598595 |
| Company Name | CURRIE MEDICAL SPECIALTIES 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00857910006307 [Primary] |
| GS1 | 00857910006802 [Package] Contains: 00857910006307 Package: CASE 10 Pr [20 Units] In Commercial Distribution |
| 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 | 2019-08-05 |
| Device Publish Date | 2019-07-26 |
| 00857910006819 | RE-CUR ALP® 3 SM THIGH - Garment (Reprocessed, Thigh, Adult) |
| 00857910006802 | RE-CUR ALP® 4 THIGH-L - Garment (Reprocessed, Thigh, Adult) |
| 00857910006796 | RE-CUR ALP® 3 THIGH-R - Garment (Reprocessed, Thigh, Adult) |
| 00857910006758 | RE-CUR ALP® 1 CALF-S - Garment (Reprocessed, Calf, Adult) |
| 00857910006741 | RE-CUR ALP® 2 CALF-XL - Garment (Reprocessed, Calf, Adult) |
| 00857910006727 | RE-CUR ALP® 2 CALF-L - Garment (Reprocessed, Calf, Adult) |
| 00857910006710 | RE-CUR ALP® 1A CALF - R - Garment (Reprocessed, Calf, Adult) |
| 00857910006703 | RE-CUR ALP® 1 CALF-R - Garment (Reprocessed, Calf, Adult) |