JUVEDERM VOLLURE XC 95661

GUDID 10888628034471

Juvéderm Vollure XC 30G 2x1.0mL

Allergan, Inc.

Dermal tissue reconstructive material, microbe-derived, anaesthetic Dermal tissue reconstructive material, microbe-derived, anaesthetic
Primary Device ID10888628034471
NIH Device Record Keyafa47a09-c250-4abf-b8a7-be6b829e98c7
Commercial Distribution StatusIn Commercial Distribution
Brand NameJUVEDERM VOLLURE XC
Version Model Number95661
Catalog Number95661
Company DUNS144796497
Company NameAllergan, 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

Customer Support Contacts

Phone8773455372
Emailaus-psreporting@allergan.com
Phone8773455372
Emailaus-psreporting@allergan.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 2 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS110888628034471 [Package]
Contains: 10888628034488
Package: Box [2 Units]
In Commercial Distribution
GS110888628034488 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LMHImplant, Dermal, For Aesthetic Use

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-06
Device Publish Date2017-03-21

Devices Manufactured by Allergan, Inc.

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