FDA UDI In Commercial Distribution 🇺🇸 United States

TriLURON

DI: M71389122087901A1 · Model: M71389122087901A13 · FIDIA FARMACEUTICI SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TriLURON
Primary DI
M71389122087901A1
Version / Model
M71389122087901A13
Catalog Number
89122-0879-01
Company Name
FIDIA FARMACEUTICI SPA
Labeler DUNS
428453013
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-04
Public Version
1
Public Version Date
2019-11-12
Public Version Status
New
Public Device Record Key
dc996787-66d3-40d8-a3c9-0ed1eea38507

Device Description

TriLURON (sodium hyaluronate) 1 prefilled syringe - 2 mL, 20mg per 2 mL

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 M71389122087901A1

Customer Contacts

Phone
866-749-2542

Premarket Submissions

Submission Number Supplement Number
P180040 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 25 Degrees Celsius