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Rumex

FDA UDI

Class II (US FDA UDI)

by Rumex International Co.

Identity

Trade Name
Rumex FDA UDI
Generic Name
Lacrimal tube FDA UDI
Device Name
"Reusable Tubing System For The Infusion Of Silicone Oil, Caprolon Adapter Adjustable To Oerlti® Orbit™, Faros™, OS3™" FDA UDI
Model / Reference
12-RTUB-4 FDA UDI
Description
"Reusable Tubing System For The Infusion Of Silicone Oil, Caprolon Adapter Adjustable To Oerlti® Orbit™, Faros™, OS3™" FDA UDI

Identifiers

Catalog Number
12-RTUB-4 FDA UDI
Primary DI / UDI-DI
00840159908525 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Lacrimal tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lacrimal tube

Rumex by Rumex International Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lacrimal tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bc2087ab-968b-4894-9126-753a6a8b822e 34 fields · synced Jun 9, 2026