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SOFT PLUG® Extended Duration Plugs

FDA UDI

Class U (US FDA UDI)

by OASIS Medical, Inc.

Identity

Trade Name
SOFT PLUG® Extended Duration Plugs FDA UDI
Generic Name
Lacrimal punctum plug FDA UDI
Device Name
SOFT PLUG® Extended Duration Plug Variety Pack 20 Plugs Assorted: 2 eaches of 0.2mm DIA x 2mm Long (GTIN: 00845819000212) 6 eaches of 0.3mm DIA x 2mm Long (GTIN: 00845819000236) 8 eaches of 0.4mm DIA x 2mm Long (GTIN: 00845819000243) 4 eaches of 0.5mm DIA x 2mm Long (GTIN: 00845819000250) FDA UDI
Model / Reference
6400V FDA UDI
Description
SOFT PLUG® Extended Duration Plug Variety Pack 20 Plugs Assorted: 2 eaches of 0.2mm DIA x 2mm Long (GTIN: 00845819000212) 6 eaches of 0.3mm DIA x 2mm Long (GTIN: 00845819000236) 8 eaches of 0.4mm DIA x 2mm Long (GTIN: 00845819000243) 4 eaches of 0.5mm DIA x 2mm Long (GTIN: 00845819000250) FDA UDI

Identifiers

Primary DI / UDI-DI
00845819000267 FDA UDI
FDA Product Code
LZU FDA UDI
GMDN Term
Lacrimal punctum plug 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Lacrimal punctum plug

SOFT PLUG® Extended Duration Plugs by OASIS Medical, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lacrimal punctum plug.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
OASIS Medical, Inc.

Sources (1)

  • FDA UDI 20e2e0d9-add6-49e3-9be2-f1334a86a9d2 34 fields · synced Jun 9, 2026