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Vivit

FDA UDI

Class II (US FDA UDI)

by 1. Vivit International Inc

Identity

Trade Name
VIVIT FDA UDI
Generic Name
Surgical/medical face mask, single-use FDA UDI
Device Name
Medical Face Mask - Earloops, Opal, 160mm Hg ASTM Level 3 FDA UDI
Model / Reference
30114EM FDA UDI
Description
Medical Face Mask - Earloops, Opal, 160mm Hg ASTM Level 3 FDA UDI

Identifiers

Primary DI / UDI-DI
10810084210045 FDA UDI
FDA Product Code
FXX FDA UDI
GMDN Term
Surgical/medical face mask, single-use 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

Yes

FDA UDI

Category: Surgical/medical face mask, single-use

Vivit by 1. Vivit International Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/medical face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 25bcbc81-a66e-408b-898e-60e52e30dcf2 34 fields · synced Jun 6, 2026