Primary Device ID | 20705031131962 |
NIH Device Record Key | 70262f4f-cd99-47e5-8792-f8e4f3ee67ab |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVA SIDEKICK LP |
Version Model Number | SDKKLPZ |
Catalog Number | SDKKLPZ |
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 | |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20705031131962 [Primary] |
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 |
20705031131962 | RELIEVA SIDEKICK SINUS GUIDE HANDLE LOW PROFILE, 1 PK |
20705031063546 | RELIEVA SIDEKICK SINUS GUIDE HANDLE LOW PROFILE |