Ritleng Hook

FDA UDI

Class I (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name: RITLENG HOOK FDA UDI
Generic Name: Transnasal lacrimal tube extractor FDA UDI
Device Name: A slender hand-held manual instrument with a hook at its distal end designed to be inserted through the nose to extract a tube, cannula, or probe previously inserted into the lacrimal drainage system (the lacrimal duct), by pulling it out through the nose. This is a reusable device. FDA UDI
Model / Reference: S1.1480 FDA UDI
Description: A slender hand-held manual instrument with a hook at its distal end designed to be inserted through the nose to extract a tube, cannula, or probe previously inserted into the lacrimal drainage system (the lacrimal duct), by pulling it out through the nose. This is a reusable device. FDA UDI

Identifiers

Primary DI / UDI-DI: 13760087126256 FDA UDI
FDA Product Code: HNQ FDA UDI
GMDN Term: Transnasal lacrimal tube extractor 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Transnasal lacrimal tube extractor

Ritleng Hook by Fci S A S Fci 20 22 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transnasal lacrimal tube extractor.

CRAWFORD HOOK — FCI S A S FCI 20 22 · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Fci S A S Fci 20 22

Sources (1)

FDA UDI ff6801a2-96f8-495c-b692-5b54efeda181 33 fields · synced Jun 6, 2026