Primary Device ID | 03607503800075 |
NIH Device Record Key | eec9703d-d6b4-4c08-a1b6-79fafc98443c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SQUALE |
Version Model Number | 380007 |
Catalog Number | 380007 |
Company DUNS | 291993439 |
Company Name | IMPLANET |
Device Count | 1 |
DM Exempt | false |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03607503800075 [Primary] |
ODP | Intervertebral Fusion Device With Bone Graft, Cervical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-14 |
Device Publish Date | 2023-06-06 |
03607505800226 | Trial Implant Holder |
03607505800219 | Trial implant W20 x D15 x H09, 4degree |
03607505800202 | Trial implant W20 x D15 x H08, 4degree |
03607505800196 | Trial implant W20 x D15 x H07, 4degree |
03607505800189 | Trial implant W20 x D15 x H06, 4degree |
03607505800172 | Trial implant W20 x D15 x H05, 4degree |
03607505800165 | Trial implant W20 x D15 x H04, 4degree |
03607505800158 | Trial implant W17 x D13 x H09, 4degree |
03607505800141 | Trial implant W17 x D13 x H08, 4degree |
03607505800134 | Trial implant W17 x D13 x H07, 4degree |
03607505800127 | Trial implant W17 x D13 x H06, 4degree |
03607505800110 | Trial implant W17 x D13 x H05, 4degree |
03607505800103 | Trial implant W17 x D13 x H04, 4degree |
03607505800097 | Trial implant W14 x D13 x H09, 4degree |
03607505800080 | Trial implant W14 x D13 x H08, 4degree |
03607505800073 | Trial implant W14 x D13 x H07, 4degree |
03607505800066 | Trial implant W14 x D13 x H06, 4degree |
03607505800059 | Trial implant W14 x D13 x H05, 4degree |
03607505800042 | Trial implant W14 x D13 x H04, 4degree |
03607505800035 | Instrumentation Box – cover |
03607505800028 | Instrumentation Box – base |
03607505800011 | Pusher |
03607505800004 | Impactor |
03607503800174 | Anterior Cervical Cage W20 x D15 x H09, 4° |
03607503800167 | Anterior Cervical Cage W20 x D15 x H08, 4° |
03607503800150 | Anterior Cervical Cage W20 x D15 x H07, 4° |
03607503800143 | Anterior Cervical Cage W20 x D15 x H06, 4° |
03607503800136 | Anterior Cervical Cage W20 x D15 x H05, 4° |
03607503800129 | Anterior Cervical Cage W20 x D15 x H04, 4° |
03607503800112 | Anterior Cervical Cage W17 x D13 x H09, 4° |
03607503800105 | Anterior Cervical Cage W17 x D13 x H08, 4° |
03607503800099 | Anterior Cervical Cage W17 x D13 x H07, 4° |
03607503800082 | Anterior Cervical Cage W17 x D13 x H06, 4° |
03607503800075 | Anterior Cervical Cage W17 x D13 x H05, 4° |
03607503800068 | Anterior Cervical Cage W17 x D13 x H04, 4° |
03607503800051 | Anterior Cervical Cage W14 x D13 x H09, 4° |
03607503800044 | Anterior Cervical Cage W14 x D13 x H08, 4° |
03607503800037 | Anterior Cervical Cage W14 x D13 x H07, 4° |
03607503800020 | Anterior Cervical Cage W14 x D13 x H06, 4° |
03607503800013 | Anterior Cervical Cage W14 x D13 x H05, 4° |
03607503800006 | Anterior Cervical Cage W14 x D13 x H04, 4° |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SQUALE 90142143 not registered Live/Pending |
Cameron Shaikh 2020-08-27 |
SQUALE 79194361 5471841 Live/Registered |
SQUALE S.r.l. 2016-09-16 |
SQUALE 72111592 0729686 Dead/Expired |
PAUL ROBERT DUBOIS 1961-01-10 |