FDA UDI In Commercial Distribution 🇺🇸 United States

JUVEDERM ULTRA PLUS XC

DI: 10888628000100 · Model: 93900 · Allergan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
JUVEDERM ULTRA PLUS XC
Primary DI
10888628000100
Version / Model
93900
Catalog Number
93900
Company Name
Allergan, Inc.
Labeler DUNS
144796497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-17
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d6914dd5-3b9e-4faf-bd22-4f19eced20e4

Device Description

Juvederm Ultra PLUS XC 27G 2x0.4mL

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LMH Implant, Dermal, For Aesthetic Use

GMDN Terms

Code Name
47887 Dermal tissue reconstructive material, microbe-derived, anaesthetic

Identifiers

Type ID
Package 30888628000104
Primary 10888628000100

Customer Contacts

Phone
8773455372

Premarket Submissions

Submission Number Supplement Number
P050047 008

Device Sizes

Type Value Unit Text
Device Size Text, specify 27G 2x0.4mL

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius