← Back to catalogue

Max Studio

FDA UDI

Class I (US FDA UDI)

by Evolutioneyes Inc

Identity

Trade Name
MAX STUDIO FDA UDI
Generic Name
Magnifying spectacles FDA UDI
Device Name
READER 3 PACK FDA UDI
Model / Reference
4128-MSR3 HYDRANGEA STRIPE FDA UDI
Description
READER 3 PACK FDA UDI

Identifiers

Primary DI / UDI-DI
00802807353996 FDA UDI
FDA Product Code
HOI FDA UDI
GMDN Term
Magnifying 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

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Magnifying spectacles

Max Studio is a highly advanced magnifying spectacle designed for individuals who are visually impaired. It features a unique combination of cutting-edge technology and innovative design, providing enhanced text enlargement and improved visual clarity. With its sleek and compact frame, Max Studio offers unparalleled convenience and accessibility.

Similar devices

Also classified as Magnifying spectacles.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Evolutioneyes Inc

Sources (1)

  • FDA UDI 1fe944c2-d246-408d-a0ea-248258d92816 33 fields · synced Jul 21, 2026