Primary Device ID | 00840828130745 |
NIH Device Record Key | 4ce55453-a930-4978-8d41-24d2499026b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LW TWINPIN,5LEAD,TELE,PINCH,51"AHA |
Version Model Number | LDW-05BT-51AS-0100 |
Catalog Number | 9023 |
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 |
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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 |
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