Primary Device ID | 00840828166836 |
NIH Device Record Key | b82bfd97-26fa-48dc-87bf-95e67b118cd7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GEN4 PLUS, DIRECT ACCESS |
Version Model Number | 5C190U-Z05800358 |
Catalog Number | 23835 |
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 | 00840828166836 [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 | 2019-04-04 |
Device Publish Date | 2019-03-27 |
00840828166706 | GEN4 PLUS, DIRECT ACCESS |
00840828166690 | GEN4 PLUS, DIRECT ACCESS |
00840828166683 | GEN4 PLUS, DIRECT ACCESS |
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