FDA UDI In Commercial Distribution 🇺🇸 United States

JUVEDERM ULTRA PLUS XC 1ML SAMPLE

DI: 10840228302770 · Model: 94155DB · Allergan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
JUVEDERM ULTRA PLUS XC 1ML SAMPLE
Primary DI
10840228302770
Version / Model
94155DB
Catalog Number
94155DB
Company Name
Allergan, Inc.
Labeler DUNS
144796497
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-10
Public Version
1
Public Version Date
2024-04-18
Public Version Status
New
Public Device Record Key
5a139399-515d-47e8-b607-6d6587673714

Device Description

JUVEDERM ULTRA PLUS XC 1ML SAMPLE

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 30840228302774
Primary 10840228302770

Customer Contacts

Phone
8773455372

Premarket Submissions

Submission Number Supplement Number
P050047 005

Device Sizes

Type Value Unit Text
Needle Gauge 27 Gauge

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius