Primary Device ID | 20705031063485 |
NIH Device Record Key | 042546ef-27a8-4766-95e8-cdb8305c00bd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVA FLEX |
Version Model Number | GC110RF |
Catalog Number | GC110RF |
Company DUNS | 361092450 |
Company Name | ACCLARENT, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Phone | +1(650)687-5888 |
xx@xx.xx |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705031063488 [Primary] |
GS1 | 20705031063485 [Package] Contains: 10705031063488 Package: BOX [5 Units] In Commercial Distribution |
KAM | CANNULA, SINUS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2016-10-01 |
20705031063263 | RELIEVA FLEX SINUS GUIDE CATHETER M-110, 1 PK |
20705031063249 | RELIEVA FLEX SINUS GUIDE CATHETER M-90, 1 PK |
20705031063225 | RELIEVA FLEX SINUS GUIDE CATHETER F-70C, 1 PK |
20705031063195 | RELIEVA FLEX SINUS GUIDE CATHETER S-0, 1 PK |
20705031063485 | RELIEVA FLEX SINUS GUIDE CATHETER M-110 |
20705031063454 | RELIEVA FLEX SINUS GUIDE CATHETER M-90 |
20705031063423 | RELIEVA FLEX SINUS GUIDE CATHETER F-70C |
20705031063379 | RELIEVA FLEX SINUS GUIDE CATHETER S-0 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() RELIEVA FLEX 77811741 4067748 Live/Registered |
Acclarent, Inc. 2009-08-24 |