Amvisc Plus

GUDID 07391899830605

0.8 ml, 1.6% Sodium Hyaluronate

Anika Therapeutics, Inc.

Vitreous/aqueous humour replacement medium, intraoperative
Primary Device ID07391899830605
NIH Device Record Key0c5101fe-b134-4001-b299-da444a98292c
Commercial Distribution StatusIn Commercial Distribution
Brand NameAmvisc Plus
Version Model Number655-806
Company DUNS807613393
Company NameAnika Therapeutics, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107391899830605 [Primary]

FDA Product Code

LZPAid, Surgical, Viscoelastic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2014-08-15

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