RibFix Titan

FDA UDI

Class II (US FDA UDI)

by Riverpoint Medical Llc

Identity

Trade Name: RibFix Titan FDA UDI
Generic Name: Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name: 60mm Intrathoracic Pre-Bent Plate, Non-Sterile, Plate: Titanium FDA UDI
Model / Reference: 323.6060 FDA UDI
Description: 60mm Intrathoracic Pre-Bent Plate, Non-Sterile, Plate: Titanium FDA UDI

Identifiers

Primary DI / UDI-DI: 00840277403001 FDA UDI
FDA Product Code: HRS FDA UDI
HTN FDA UDI
GMDN Term: Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

RibFix Titan by Riverpoint Medical Llc — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Riverpoint Medical Llc

Sources (1)

FDA UDI 4c9e3088-b59b-455c-8580-9dd7ac37f91b 33 fields · synced Jun 1, 2026