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Plasdent ULTRAPROOF Earloop Mask

FDA UDI

Class II (US FDA UDI)

by Plasdent Corp.

Identity

Trade Name
Plasdent ULTRAPROOF Earloop Mask FDA UDI
Generic Name
Surgical/medical respirator, antimicrobial FDA UDI
Device Name
ULTRAPROOF (TM) Earloop Mask with Shield- Pink (25pcs/box) FDA UDI
Model / Reference
MKS1 FDA UDI
Description
ULTRAPROOF (TM) Earloop Mask with Shield- Pink (25pcs/box) FDA UDI

Identifiers

Catalog Number
MKS3-2 FDA UDI
Primary DI / UDI-DI
D832MKS32 FDA UDI
510(k) Number
K133070 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical respirator, antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

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: Surgical/medical respirator, antimicrobial

Plasdent ULTRAPROOF Earloop Mask by Plasdent Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical respirator, antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Plasdent Corp.

Sources (1)

  • FDA UDI 4d1909a9-3b39-4eb1-a1da-de4f4cb5645e 35 fields · synced May 31, 2026