FDA UDI In Commercial Distribution 🇺🇸 United States

Euflexxa

DI: 07640128544210 · Model: 4100 · FERRING PHARMACEUTICALS INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
Euflexxa
Primary DI
07640128544210
Version / Model
4100
Company Name
FERRING PHARMACEUTICALS INC.
Labeler DUNS
103722955
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2014-09-24
Public Version
4
Public Version Date
2023-11-27
Public Version Status
Update
Public Device Record Key
58bc7279-f90e-40c8-88bc-1d8e67767d6f

Device Description

1% sodium hyaluronate

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
MOZ Acid, hyaluronic, intraarticular

GMDN Terms

Code Name
44757 Synovial fluid supplementation medium

Identifiers

Type ID
Primary 07640128544210
Unit of Use 07640128544302

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify ml

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Do Not Freeze
Type
Storage Environment Temperature
Temperature Range
36 – 77 Degrees Fahrenheit