Primary Device ID | 04719873695218 |
NIH Device Record Key | b16334c2-3f7b-4560-a69c-a89d7a8581ee |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | S1001-2220 |
Company DUNS | 658863238 |
Company Name | CARILEX 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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 04719873695201 [Primary] |
GS1 | 04719873695218 [Package] Contains: 04719873695201 Package: [10 Units] In Commercial Distribution |
GS1 | 04719873695225 [Package] Package: [5 Units] In Commercial Distribution |
OMP | Negative Pressure Wound Therapy Powered Suction Pump |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-04-01 |
Device Publish Date | 2020-03-24 |
04719873691296 - NA | 2024-04-30 VT•200-i SYS Global Carilex |
04719873695898 - NA | 2024-04-30 VT•200-i NX SYS Global Carilex |
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 |