Primary Device ID | 00840828194235 |
NIH Device Record Key | 86706b16-b63e-4453-957d-12c754eae1cc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | REGO 1.1,PID,WT,PN,TL,FD,10' |
Version Model Number | PD11-100400000A |
Catalog Number | 27854 |
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 |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com | |
Phone | 18002357500 |
mwinter@curbell.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840828194235 [Primary] |
ILQ | System, Communication, 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 | 2025-03-07 |
Device Publish Date | 2025-02-27 |