FDA UDI In Commercial Distribution 🇺🇸 United States

Synvisc One

DI: 05060604130034 · Model: NA · ACRE PHARMA LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Synvisc One
Primary DI
05060604130034
Version / Model
NA
Company Name
ACRE PHARMA LIMITED
Labeler DUNS
218668297
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-27
Public Version
2
Public Version Date
2018-07-27
Public Version Status
Update
Public Device Record Key
68b6820a-cd06-407a-8d55-c9dcf6f7f686

Device Description

Inject into the knee to relieve the pain from osteoarthritis.

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
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
MOZ Acid, Hyaluronic, Intraarticular

GMDN Terms

Code Name
44757 Synovial fluid supplementation medium

Identifiers

Type ID
Primary 05060604130034

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius