Primary Device ID | 00866142000014 |
NIH Device Record Key | a4bedb48-8276-462e-9ab3-8c909f9fcfb3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Elevess |
Version Model Number | 685-310 |
Company DUNS | 807613393 |
Company Name | Anika Therapeutics, 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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00866142000014 [Primary] |
LMH | Implant, Dermal, For Aesthetic Use |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-30 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ELEVESS 77028188 not registered Dead/Abandoned |
ANIKA THERAPEUTICS, INC. 2006-10-24 |
![]() ELEVESS 77018057 3509169 Dead/Cancelled |
ANIKA THERAPEUTICS, INC. 2006-10-10 |