Primary Device ID | 00840828139847 |
NIH Device Record Key | b6820092-f181-4214-995e-32278879c19f |
Commercial Distribution Discontinuation | 2017-12-28 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | CBL 060,GE,MULTI,10LD,YOKE,10FT,AH,INTER |
Version Model Number | CBT-10NR-10CM-3001 |
Catalog Number | 18675 |
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 |