Lacriflow

FDA UDI

Class U (US FDA UDI)

by Kaneka Corp.

Identity

Trade Name: LACRIFLOW FDA UDI
Generic Name: Lacrimal tube FDA UDI
Device Name: The LACRIFLOW is indicated in treatments of epiphora in-patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction. FDA UDI
Model / Reference: LF-R105A FDA UDI
Description: The LACRIFLOW is indicated in treatments of epiphora in-patients 12 months and older, in cases of: - Canalicular pathologies (stenosis, obstruction, lacerations), - During Dacryocystorhinostomy (conventional or laser), - Congenital nasolacrimal duct obstruction. FDA UDI

Identifiers

Primary DI / UDI-DI: 04540778140868 FDA UDI
FDA Product Code: OKS FDA UDI
GMDN Term: Lacrimal tube FDA UDI

Classification

Device Class: U FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Length — 105 Millimeter FDA UDI

Category: Lacrimal tube

Lacriflow by Kaneka Corp. — Class U — 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 U	Pending data

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Manufacturer

Manufacturer: Kaneka Corp.

Sources (1)

FDA UDI 257d65a8-23e2-4ce0-a283-b69482c24ba8 36 fields · synced Jun 8, 2026