| Primary Device ID | 04713616092579 |
| NIH Device Record Key | 8ce269da-0dfc-4d14-a5f5-4a7e0b429b4a |
| Commercial Distribution Discontinuation | 2018-09-18 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | S2201-A160 |
| Company DUNS | 658863238 |
| Company Name | CARILEX 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04713616092579 [Package] Contains: 04713616093408 Package: [10 Units] Discontinued: 2018-09-18 Not in Commercial Distribution |
| GS1 | 04713616093408 [Primary] |
| FNM | Mattress, Air Flotation, Alternating Pressure |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-09-18 |
| Device Publish Date | 2017-03-22 |
| 04719873696857 - NA | 2023-12-12 VT•200 P.U. Global Med One |
| 04719873696864 - NA | 2023-12-12 VT•200 SYS Global Med One |
| 14713616094785 - NA | 2023-09-18 Envelop Cover 42'' × 80'' QLT-1p |
| 04713616094764 - NA | 2023-09-06 Envelop M-set 42'' × 80'' QLT Carilex |
| 04719873692972 - NA | 2022-08-23 TheraFlo 9 M-set 90 x 200cm WDTX Carilex |
| 00471987369297 - NA | 2022-08-01 TheraFlo 9 M-set 90 x 200cm WDTX Carilex |
| 04719873692989 - NA | 2022-08-01 TheraFlo 9 M-set 107 x 200cm DTX Carilex |
| 04719873693108 - NA | 2022-08-01 TheraFlo 7 & 9 Cover 90 x 200cm WDTX Carilex-1p |