Aveo Hello

FDA UDI

Class II (US FDA UDI)

by Supervision Optimax Sdn. Bhd.

Identity

Trade Name: Aveo Hello FDA UDI
Generic Name: Soft corrective contact lens, daily-disposable FDA UDI
Device Name: Daily Disposable Soft Contact Lenses FDA UDI
Model / Reference: - 2.25 D FDA UDI
Description: Daily Disposable Soft Contact Lenses FDA UDI

Identifiers

Primary DI / UDI-DI: 09555774922795 FDA UDI
FDA Product Code: MVN FDA UDI
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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Soft corrective contact lens, daily-disposable

Aveo Hello by Supervision Optimax Sdn. Bhd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

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1-Day Flat Pack CP30 BC840 — MENICON CO., LTD. · Class II
Miru 1day Menicon Flat Pack TC CP90 — MENICON CO., LTD. · Class II
Miru 1day Menicon Flat Pack TC CP90 — MENICON CO., LTD. · Class II
1-Day Flat Pack CP30 — MENICON CO., LTD. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Supervision Optimax Sdn. Bhd.

Sources (1)

FDA UDI 2a66eed3-1a18-4dce-9a14-7ef871504617 33 fields · synced Jun 8, 2026