Primary Device ID | 00840828193221 |
NIH Device Record Key | a645a4d5-e8af-4582-a392-6d93cbe3e440 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GEN4 DIGITAL |
Version Model Number | 4D120N-Z10402H |
Catalog Number | 29371 |
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 | true |
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 |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com | |
Phone | 1-800-235-7500 |
mwinter@curbell.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840828193221 [Primary] |
IQA | System, Environmental Control, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-18 |
Device Publish Date | 2024-11-08 |