FDA UDI In Commercial Distribution 🇺🇸 United States

RHA® Redensity

DI: 07640173234197 · Model: RHA® Redensity US 1ml Schott/2 aig. Terumo TW30G1/2 · Teoxane SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RHA® Redensity
Primary DI
07640173234197
Version / Model
RHA® Redensity US 1ml Schott/2 aig. Terumo TW30G1/2
Catalog Number
940056/02
Company Name
Teoxane SA
Labeler DUNS
482411860
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-15
Public Version
1
Public Version Date
2023-09-25
Public Version Status
New
Public Device Record Key
ee72f25c-411d-4578-87ab-8df28cf1a779

Device Description

"One box of RHA® Redensity contains two blisters and one instruction for use. Each blister contains a 1mL prefilled syringe and two needles (30G 1/2). Box Packaging (ID 07640173234180) is defined as unit of sales and identified with a serial number."

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

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
Primary 07640173234197

Customer Contacts

Phone
877-373-8669

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Special Storage Condition, Specify: Store at room temperature (up to 25°C / 77°F). Do not expose to direct sunlight. Do not freeze.