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Flents

FDA UDI

Class U (US FDA UDI)

by Apothecary Products, Inc.

Identity

Trade Name
Flents FDA UDI
Generic Name
Eye wash cup FDA UDI
Device Name
PLASTIC EYE WASH CUP FDA UDI
Model / Reference
68354/68354CA FDA UDI
Description
PLASTIC EYE WASH CUP FDA UDI

Identifiers

Primary DI / UDI-DI
00025715683546 FDA UDI
FDA Product Code
LXQ FDA UDI
GMDN Term
Eye wash cup FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Eye wash cup

Flents by Apothecary Products, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye wash cup.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 47cd71c5-8771-459a-b597-426de21a2074 34 fields · synced May 30, 2026