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Triluron

FDA UDI

Class III (US FDA UDI)

by Fidia Farmaceutici

Identity

Trade Name
TRILURON FDA UDI
Generic Name
Synovial fluid supplementation medium FDA UDI
Device Name
TRILURON (sodium hyaluronate) 1 prefilled syringe - 2 mL, 20mg per 2 mL FDA UDI
Model / Reference
89122-0879-01 FDA UDI
Description
TRILURON (sodium hyaluronate) 1 prefilled syringe - 2 mL, 20mg per 2 mL FDA UDI

Identifiers

Catalog Number
89122-0879-01 FDA UDI
Primary DI / UDI-DI
M713891220879010 FDA UDI
PMA Number
P180040 FDA UDI
FDA Product Code
MOZ FDA UDI
GMDN Term
Synovial fluid supplementation medium FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synovial fluid supplementation medium

Triluron by Fidia Farmaceutici — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synovial fluid supplementation medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fidia Farmaceutici

Sources (1)

  • FDA UDI ffde2992-a8d8-4116-8efe-d43ba5b16a0a 37 fields · synced Jun 1, 2026