JUVEDERM ULTRA PLUS XC 93900

GUDID 30888628000104

Dermal tissue reconstructive material, microbe-derived, anaesthetic Dermal tissue reconstructive material, microbe-derived, anaesthetic

Primary Device ID	30888628000104
NIH Device Record Key	d6914dd5-3b9e-4faf-bd22-4f19eced20e4
Commercial Distribution Status	In Commercial Distribution
Brand Name	JUVEDERM ULTRA PLUS XC
Version Model Number	93900
Catalog Number	93900
Company DUNS	144796497
Company Name	Allergan, 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

Phone	8773455372
Email	aus-psreporting@allergan.com
Phone	8773455372
Email	aus-psreporting@allergan.com

Device Size Text, specify	0
Device Size Text, specify	0

Storage Environment Temperature	Between 2 Degrees Celsius and 25 Degrees Celsius
Storage Environment Temperature	Between 2 Degrees Celsius and 25 Degrees Celsius

Device Issuing Agency	Device ID
GS1	10888628000100 [Primary]
GS1	30888628000104 [Package] Contains: 10888628000100 Package: Box [2 Units] In Commercial Distribution

LMH	Implant, Dermal, For Aesthetic Use

Steralize Prior To Use	false
Device Is Sterile	true