FDA UDI In Commercial Distribution 🇺🇸 United States

Revanesse Versa 1.2 mL

DI: 10669808001021 · Model: 40089 · Prollenium Medical
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Revanesse Versa 1.2 mL
Primary DI
10669808001021
Version / Model
40089
Company Name
Prollenium Medical
Labeler DUNS
247326606
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-15
Public Version
2
Public Version Date
2023-08-16
Public Version Status
Update
Public Device Record Key
a8384673-d626-46fe-82fb-1d5a78a7e3d9

Device Description

Revanesse Versa is manufactured by Prollenium Medical Technologies, and is a biocompatible, sterile, injectable hydrogel based on bioresorbable cross-linked hyaluronan (HA) (22 – 28 mg / mL concentration). The gel is delivered in a pre-filled disposable glass syringe. Each box of Revanesse Versa contains two 1.2 mL syringes of Revanesse Versa along with two sterile needles. Revanesse Versa is injected by qualified, trained doctors into the dermis of patients, using a variety of techniques. The injections place a small portion of the gel beneath a crease or wrinkle in the skin and the augmentation of the tissue produces a smoothing effect on the surface.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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

GMDN Terms

Code Name
61219 Dermal tissue reconstructive material, synthetic polymer, bioabsorbable

Identifiers

Type ID
Primary 10669808001021