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Diamatrix

FDA UDI

Class U (US FDA UDI)

by Diamatrix

Identity

Trade Name
Diamatrix FDA UDI
Generic Name
Lacrimal punctum plug FDA UDI
Device Name
DACRIOS .8mm Silicone Punctal Plug, Box of 2 FDA UDI
Model / Reference
DPPS08 FDA UDI
Description
DACRIOS .8mm Silicone Punctal Plug, Box of 2 FDA UDI

Identifiers

Catalog Number
DPPS08 FDA UDI
Primary DI / UDI-DI
00813059017642 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Lacrimal punctum plug

Diamatrix by Diamatrix — 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
Diamatrix

Sources (1)

  • FDA UDI 6ef054e6-8171-4086-85d1-565de2e5c47f 35 fields · synced May 31, 2026