Primary Device ID | 10705031063358 |
NIH Device Record Key | 86aa68ac-f01f-4763-8a88-14d4d69f1504 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RELIEVA LUMA |
Version Model Number | SISLGCAWOLF |
Catalog Number | SISLGCAWOLF |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry, clean and safe place at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705031063358 [Primary] |
EQH | SOURCE, CARRIER, FIBEROPTIC LIGHT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10705031063358]
Hydrogen Peroxide;Moist Heat or Steam Sterilization;High-level Disinfectant
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2017-09-01 |
20705031135670 | RELIEVA LUMA LIGHT GUIDE CABLE 2 |
10705031205895 | RELIEVA LUMA LIGHT GUIDE CABLE ADAPTER - STORZ |
10705031135680 | RELIEVA LUMA LIGHT GUIDE CABLE ADAPTER - OLYMPUS |
10705031063358 | RELIEVA LUMA LIGHT GUIDE CABLE ADAPTER - WOLF / DYONICS |
10705031063341 | RELIEVA LUMA LIGHT GUIDE CABLE ADAPTER - ACMI / STRYKER |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() RELIEVA LUMA 77133129 3595414 Live/Registered |
Acclarent, Inc. 2007-03-16 |