Hubble Digital Vision

FDA UDI

Class I (US FDA UDI)

by Cao Group, Inc.

Identity

Trade Name: Hubble Digital Vision FDA UDI
Generic Name: General-purpose surgical microscope FDA UDI
Device Name: Battery powered electronic magnification loupe and display system for use in clinical settings. FDA UDI
Model / Reference: 005-00109 FDA UDI
Description: Battery powered electronic magnification loupe and display system for use in clinical settings. FDA UDI

Identifiers

Primary DI / UDI-DI: 00872320006471 FDA UDI
FDA Product Code: EPT FDA UDI
GMDN Term: General-purpose surgical microscope FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4700 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

Yes

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose surgical microscope

Hubble Digital Vision by Cao Group, 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: Cao Group, Inc.

Sources (1)

FDA UDI d0b73258-7f11-451a-8d75-a1aad227dec1 34 fields · synced Jun 6, 2026