FDA UDI In Commercial Distribution 🇺🇸 United States

Sculptra

DI: 00302995961077 · Model: 2 vial pack · GALDERMA LABORATORIES, L.P.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sculptra
Primary DI
00302995961077
Version / Model
2 vial pack
Company Name
GALDERMA LABORATORIES, L.P.
Labeler DUNS
047350186
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-14
Public Version
2
Public Version Date
2023-12-11
Public Version Status
Update
Public Device Record Key
775d8e6f-de70-41b9-b0ff-ea1f030344c8

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
59133 Dermal tissue reconstructive material, synthetic mineral

Identifiers

Type ID
Primary 00302995961077

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do not freeze
Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature up to 30°C (86°F)