FDA UDI In Commercial Distribution 🇺🇸 United States

JUVEDERM ULTRA

DI: 10888628044746 · Model: 96206 · Allergan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
JUVEDERM ULTRA
Primary DI
10888628044746
Version / Model
96206
Catalog Number
96206
Company Name
Allergan, Inc.
Labeler DUNS
144796497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-22
Public Version
1
Public Version Date
2019-04-30
Public Version Status
New
Public Device Record Key
084c4131-2e7f-44de-b222-bca31f22b4eb

Device Description

Juvéderm ULTRA 2x0.55mL

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
59131 Dermal tissue reconstructive material, microbe-derived

Identifiers

Type ID
Package 10888628044739
Primary 10888628044746

Customer Contacts

Phone
8773455372

Premarket Submissions

Submission Number Supplement Number
P050047 066

Device Sizes

Type Value Unit Text
Device Size Text, specify 30G 2x0.55mL

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius