Primary Device ID | 20705031206318 |
NIH Device Record Key | 29ade4b7-6e17-4b53-955e-bf9602db7554 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVA SPIN |
Version Model Number | RS0516M |
Catalog Number | RS0516M |
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 | |
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 |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool, dry place |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705031206311 [Primary] |
GS1 | 20705031206318 [Package] Contains: 10705031206311 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 | 4 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2016-10-01 |
20705031230580 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT, 1 PK |
20705031230566 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT, 1 PK |
20705031227580 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110C SINUS GUIDE CATHETER TIP, 1 PK |
20705031206370 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT, 1 PK |
20705031206325 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT, 1 PK |
20705031206042 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110 SINUS GUIDE CATHETER TIP, 1 PK |
20705031206011 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, S-0 SINUS GUIDE CATHETER TIP, 1 PK |
20705031200576 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 M-110 GUIDE KIT, 1 PK |
20705031200545 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT, 1 PK |
20705031200538 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, F-70 SINUS GUIDE CATHETER TIP, 1 PK |
20705031230597 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT |
20705031230573 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT |
20705031227573 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110C SINUS GUIDE CATHETER TIP |
20705031206318 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT |
20705031206301 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT |
20705031206035 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, M-110 SINUS GUIDE CATHETER TIP |
20705031206028 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, S-0 SINUS GUIDE CATHETER TIP |
20705031200583 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, F-70 SINUS GUIDE CATHETER TIP |
20705031200569 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 M-110 GUIDE KIT |
20705031200552 | RELIEVA SPIN BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() RELIEVA SPIN 85436310 4335661 Dead/Cancelled |
ACCLARENT, INC. 2011-09-30 |