Primary Device ID | 04713616094764 |
NIH Device Record Key | 5a673801-2b38-4c20-85cc-64097a4d3fd8 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | S2003-2150 |
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 | false |
Serial Number | true |
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 | 04713616094764 [Primary] |
FNM | Mattress, Air Flotation, Alternating Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-06 |
Device Publish Date | 2023-08-29 |
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 | 2023-09-06Envelop M-set 42'' × 80'' QLT Carilex |
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 |