FDA UDI In Commercial Distribution 🇺🇸 United States

RHA® 3

DI: 07640173230045 · Model: RHA® 3 (1mL) · Teoxane SA
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
RHA® 3
Primary DI
07640173230045
Version / Model
RHA® 3 (1mL)
Catalog Number
940008
Company Name
Teoxane SA
Labeler DUNS
482411860
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-30
Public Version
4
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
f0117c68-3165-47bb-8801-192753f8171a
Distribution End Date
2025-02-21

Device Description

One box of RHA® 3 contains two blisters and one instruction for use. Each blister contains a 1mL prefilled syringe and two needles (27G 1/2). Box Packaging (ID 07640173230038) 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
Yes
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 07640173230038
Primary 07640173230045

Customer Contacts

Phone
877-373-8669

Storage Conditions

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