Primary Device ID | 00840828157551 |
NIH Device Record Key | cf07c0b1-7d55-4bf3-9e54-8f40e49cee1a |
Commercial Distribution Discontinuation | 2018-07-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | 800,102 P37,R4,BE,2L,STKR |
Version Model Number | IC-0856 |
Catalog Number | 7807 |
Company DUNS | 796452311 |
Company Name | CURBELL MEDICAL PRODUCTS, 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 | 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 | false |
OTC Over-The-Counter | false |