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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 surgical instrument handle quick lock adaptor FDA UDI
Device Name
Flushing Adapter For Vitreoretinal Tips, Titanium FDA UDI
Model / Reference
12-000T FDA UDI
Description
Flushing Adapter For Vitreoretinal Tips, Titanium FDA UDI

Identifiers

Catalog Number
12-000T FDA UDI
Primary DI / UDI-DI
00840159902455 FDA UDI
FDA Product Code
IQG FDA UDI
GMDN Term
Ophthalmic surgical instrument handle quick lock adaptor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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 surgical instrument handle quick lock adaptor

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

Similar devices

Also classified as Ophthalmic surgical instrument handle quick lock adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6365d0c3-f21e-4ac0-994f-f4cae48a19f3 34 fields · synced Jun 9, 2026