FDA UDI In Commercial Distribution 🇺🇸 United States

Orthovisc

DI: 10886705023110 · Model: 630-254 · Anika Therapeutics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Orthovisc
Primary DI
10886705023110
Version / Model
630-254
Company Name
Anika Therapeutics, Inc.
Labeler DUNS
807613393
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-08-15
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
482493e8-48bc-4ad7-8626-7283323ffb06

Device Description

2 mL, 15 mg/mL High Molecular weight Hyaluronan

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 10886705023110

Premarket Submissions

Submission Number Supplement Number
P030019 000