RELIEVA FLEX GC070CRF
GUDID 20705031063423
RELIEVA FLEX SINUS GUIDE CATHETER F-70C
ACCLARENT, INC.
Paranasal sinus guide-catheter| Primary Device ID | 20705031063423 |
| NIH Device Record Key | 1b1894c2-736a-45bb-ba1b-5aea044fc896 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RELIEVA FLEX |
| Version Model Number | GC070CRF |
| Catalog Number | GC070CRF |
| 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 |
Customer Support Contacts
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(877)775-2789 |
| xx@xx.xx | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
| Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10705031063426 [Primary] |
| GS1 | 20705031063423 [Package] Contains: 10705031063426 Package: BOX [5 Units] In Commercial Distribution |
FDA Product Code
| KAM | CANNULA, SINUS |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-22 |
| Device Publish Date | 2016-10-01 |
On-Brand Devices [RELIEVA FLEX]
| 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 |
Trademark Results [RELIEVA FLEX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RELIEVA FLEX 77811741 4067748 Live/Registered |
Acclarent, Inc. 2009-08-24 |
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