Primary Device ID | 04713616094634 |
NIH Device Record Key | 3d8cf4b3-12ba-4ac2-85fe-056288085278 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | S1001-8200 |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04713616094627 [Primary] |
GS1 | 04713616094634 [Package] Contains: 04713616094627 Package: [5 Units] In Commercial Distribution |
GS1 | 04713616094641 [Package] Package: [6 Units] In Commercial Distribution |
OMP | Negative Pressure Wound Therapy Powered Suction Pump |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-24 |
Device Publish Date | 2021-03-16 |
04719873696901 - NA | 2024-06-28 TheraFlo 9 M-set 36" x 80" WDTX Carilex |
14719873696915 - NA | 2024-06-28 TheraFlo 9 Cover 36" x 80" WDTX Carilex-1p |
04719873696925 - NA | 2024-06-28 TheraFlo 9 M-set 42" x 80" DTX Carilex |
14719873696939 - NA | 2024-06-28 TheraFlo 9 Cover 42" x 80" DTX Carilex-1p |
04719873696949 - NA | 2024-06-28 FIT M-Set 36" x 80" VTX Carilex |
04719873696956 - NA | 2024-06-28 FIT M-Set 36" x 80" WDTX Carilex |
04719873696963 - NA | 2024-06-28 FIT M-set 36" x 80" QLT Carilex |
04719873696970 - NA | 2024-06-28 FIT M-Set 42" x 80" VTX Carilex |