Primary Device ID | 00840828181709 |
NIH Device Record Key | 791852d1-170d-48af-9ba5-eb76af8e155e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3601 P37,1TO1,NO PIN 32,STKR |
Version Model Number | 521209900942 |
Catalog Number | 26363 |
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 | 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 | 00840828181709 [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 | 2020-10-15 |
Device Publish Date | 2020-10-07 |
00840828100656 | 3601 P37,1TO1,NO PIN 32,STKR |
00840828181365 | 3601 P37,1TO1,NO PIN 32,STKR |
00840828181709 | 3601 P37,1TO1,NO PIN 32,STKR |