Primary Device ID | 00840828170000 |
NIH Device Record Key | 7ef48994-6e03-47d9-b8fe-a7cfeeccbee1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GEN4 PLUS, DIRECT ACCESS |
Version Model Number | 5C331U-P00500028 |
Catalog Number | 24150 |
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 | 18002357500 |
mwinter@curbell.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840828170000 [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 | 2019-04-09 |
Device Publish Date | 2019-04-01 |
00840828166706 | GEN4 PLUS, DIRECT ACCESS |
00840828166690 | GEN4 PLUS, DIRECT ACCESS |
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