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Miru 1day Menicon Flat Pack refill30

FDA UDI

Class II (US FDA UDI)

by Menicon Co., Ltd.

Identity

Trade Name
Miru 1day Menicon Flat Pack refill30 FDA UDI
Generic Name
Soft corrective contact lens, daily-disposable FDA UDI
Model / Reference
-4.00 FDA UDI

Identifiers

Primary DI / UDI-DI
00884465018417 FDA UDI
FDA Product Code
LPL 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
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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Soft corrective contact lens, daily-disposable

Miru 1day Menicon Flat Pack refill30 by Menicon Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft corrective contact lens, daily-disposable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Menicon Co., Ltd.

Sources (1)

  • FDA UDI 4e331a6e-f332-4ec8-996e-e85d36b59999 32 fields · synced May 31, 2026