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
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Fidia Farmaceutici
Sources (1)
- FDA UDI ffde2992-a8d8-4116-8efe-d43ba5b16a0a 37 fields · synced Jun 1, 2026