Primary Device ID | 00840828130332 |
NIH Device Record Key | fb5fe49c-356f-4393-847f-b149f8b2ae94 |
Commercial Distribution Discontinuation | 2016-10-14 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | LW PLP2000,5LEAD,TELE,SNAP,29"AHA |
Version Model Number | LDW-05AU-29AS-0000 |
Catalog Number | 8939 |
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 |