Primary Device ID | 00840828125192 |
NIH Device Record Key | 27118662-4107-4946-8e7a-97cfe63c7c11 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CBL 024,PLP,MLD,3LEAD,SNAP,10FT,AHA |
Version Model Number | CBM-03JA-10AS-0121 |
Catalog Number | 5616 |
Company DUNS | 796452311 |
Company Name | CURBELL MEDICAL PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
00840828182294 - REUS,NCLR OXSMRT SPO2 SNSR,9.5',LG CLAM | 2024-04-18 REUS,NCLR OXSMRT SPO2 SNSR,9.5',LG CLAM |
00840828182300 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG CLAM | 2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG CLAM |
00840828182317 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG SOFT | 2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',LG SOFT |
00840828182324 - REUS,NLCR OXSMRT SPO2 SNSR,3.3',SM SOFT | 2024-04-18 REUS,NLCR OXSMRT SPO2 SNSR,3.3',SM SOFT |
00840828182331 - REUS,NLCR OXMAX SPO2 SNSR,9.5',LG CLAM | 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,9.5',LG CLAM |
00840828182348 - REUS,NLCR OXMAX SPO2 SNSR,3.3',LG CLAM | 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,3.3',LG CLAM |
00840828182355 - REUS,NLCR OXMAX SPO2 SNSR,9.5',LG SOFT | 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,9.5',LG SOFT |
00840828182362 - REUS,NLCR OXMAX SPO2 SNSR,3.3',LG SOFT | 2024-04-18 REUS,NLCR OXMAX SPO2 SNSR,3.3',LG SOFT |