FDA UDI In Commercial Distribution 🇺🇸 United States

Restylane Defyne

DI: 00302995965129 · Model: Gel 1 mL Syringe · Q-Med AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Restylane Defyne
Primary DI
00302995965129
Version / Model
Gel 1 mL Syringe
Company Name
Q-Med AB
Labeler DUNS
355371873
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-13
Public Version
1
Public Version Date
2022-12-21
Public Version Status
New
Public Device Record Key
9942dac1-c9cb-4860-bffb-0f08390f38fb

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
Primary 00302995965129

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
– 25 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
– 77 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Do not expose to direct sunlight
Type
Special Storage Condition, Specify
Special Conditions
Do not freeze
Type
Special Storage Condition, Specify
Special Conditions
Refrigeration not required