Primary Device ID | 20705031200293 |
NIH Device Record Key | 4115df4b-6829-459a-990f-9a9be34d88e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVA ULTIRRA |
Version Model Number | BC0724RU |
Catalog Number | BC0724RU |
Company DUNS | 361092450 |
Company Name | ACCLARENT, INC. |
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 | 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(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(877)775-2789 |
xx@xx.xx |
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 Issuing Agency | Device ID |
---|---|
GS1 | 10705031200296 [Primary] |
GS1 | 20705031200293 [Package] Contains: 10705031200296 Package: BOX [5 Units] In Commercial Distribution |
LRC | INSTRUMENT, ENT MANUAL SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2016-10-01 |
20705031200293 | RELIEVA ULTIRRA SINUS BALLOON CATHETER 7x24 |
20705031200286 | RELIEVA ULTIRRA SINUS BALLOON CATHETER 7x16 |
20705031200279 | RELIEVA ULTIRRA SINUS BALLOON CATHETER 6x16 |
20705031200255 | RELIEVA ULTIRRA SINUS BALLOON CATHETER 5x16 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() RELIEVA ULTIRRA 85393116 4227217 Live/Registered |
ACCLARENT, INC. 2011-08-09 |