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Rumex

FDA UDI

Class I (US FDA UDI)

by Rumex International Co.

Identity

Trade Name
Rumex FDA UDI
Generic Name
Ophthalmic cannula transscleral trocar blade FDA UDI
Device Name
Disposable One Step Trocar System 25 Ga (1 Set Of 3 Insert Handles And 1 Infusion Line), 6 Per Box FDA UDI
Model / Reference
12-5244 FDA UDI
Description
Disposable One Step Trocar System 25 Ga (1 Set Of 3 Insert Handles And 1 Infusion Line), 6 Per Box FDA UDI

Identifiers

Catalog Number
12-5244 FDA UDI
Primary DI / UDI-DI
00840159908471 FDA UDI
FDA Product Code
NGY FDA UDI
GMDN Term
Ophthalmic cannula transscleral trocar blade FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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: Ophthalmic cannula transscleral trocar blade

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

Similar devices

Also classified as Ophthalmic cannula transscleral trocar blade.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rumex International Co.

Sources (1)

  • FDA UDI 2ed8eab8-1d50-40c0-b635-0f9758799f9a 34 fields · synced Jun 9, 2026