Primary Device ID | 10603295551270 |
NIH Device Record Key | 30ddd02d-d670-4519-abf2-98c2e028b023 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CUPTIMIZE |
Version Model Number | 451580054 |
Catalog Number | 451580054 |
Company DUNS | 080506581 |
Company Name | DEPUY ORTHOPAEDICS, INC. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10603295551270 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-25 |
Device Publish Date | 2022-07-15 |
10603295551287 | Cuptimize for Windows |
10603295551270 | Cuptimize for Ios |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CUPTIMIZE 97296378 not registered Live/Pending |
Depuy Synthes Products, Inc. 2022-03-04 |
CUPTIMIZE 97200726 not registered Live/Pending |
Cuptimize, Inc. 2022-01-03 |
CUPTIMIZE 90013955 not registered Live/Pending |
RAD2U, Inc. 2020-06-22 |