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PolyVue HD Dailies

FDA UDI

Class II (US FDA UDI)

by Interojo Inc.

Identity

Trade Name
PolyVue HD Dailies FDA UDI
Generic Name
Soft corrective contact lens, daily-disposable FDA UDI
Model / Reference
HD Dailies FDA UDI

Identifiers

Primary DI / UDI-DI
08806392000770 FDA UDI
FDA Product Code
MVN FDA UDI
GMDN Term
Soft corrective contact lens, daily-disposable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.5925 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

PolyVue HD Dailies by Interojo Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Interojo Inc.

Sources (1)

  • FDA UDI aa54373c-33f5-4c4e-b59e-7f4dfdfdb80b 35 fields · synced May 30, 2026