read on

FDA UDI

Class I (US FDA UDI)

by Read On Inc.

Identity

Trade Name: read on FDA UDI
Generic Name: Prescription spectacles FDA UDI
Device Name: 3 mm eyewear, purple, +2.0 dpt, 2 units in paper box incl. leaflet FDA UDI
Model / Reference: 7640288790816 FDA UDI
Description: 3 mm eyewear, purple, +2.0 dpt, 2 units in paper box incl. leaflet FDA UDI

Identifiers

Primary DI / UDI-DI: 07640288790816 FDA UDI
FDA Product Code: HOI FDA UDI
GMDN Term: Prescription spectacles FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.5840 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Prescription spectacles

read on by Read On Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Read On Inc.

Sources (1)

FDA UDI 56bf8a20-ee90-4eb2-95b7-697a58e379e9 33 fields · synced May 30, 2026