Primary Device ID | 20705031232911 |
NIH Device Record Key | f49906ba-dfae-4451-ba3f-1ebf007aca30 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVA SPINPLUS |
Version Model Number | RSP0616F |
Catalog Number | RSP0616F |
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(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
xx@xx.xx | |
Phone | +1(650)687-5888 |
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 | 10705031232914 [Primary] |
GS1 | 20705031232911 [Package] Contains: 10705031232914 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 |
20705031233062 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 NO GUIDE KIT, 1 PK |
20705031233048 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 NO GUIDE KIT, 1 PK |
20705031232928 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 M-110C GUIDE KIT, 1 PK |
20705031232904 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT, 1 PK |
20705031232867 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT, 1 PK |
20705031232843 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT, 1 PK |
20705031232829 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT, 1 PK |
20705031232812 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT, 1 PK |
20705031233055 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 NO GUIDE KIT |
20705031233031 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 NO GUIDE KIT |
20705031232935 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 M-110C GUIDE KIT |
20705031232911 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 F-70 GUIDE KIT |
20705031232874 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 M-110C GUIDE KIT |
20705031232850 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 F-70 GUIDE KIT |
20705031232836 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 5x16 3 GUIDE KIT |
20705031232386 | RELIEVA SPINPLUS BALLOON SINUPLASTY SYSTEM, 6x16 3 GUIDE KIT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() RELIEVA SPINPLUS 86487044 4886857 Live/Registered |
ACCLARENT, INC. 2014-12-19 |