← Back to catalogue

ARveo

FDA UDI

Class I (US FDA UDI)

by Leica Microsystems (Schweiz) AG

Identity

Trade Name
ARveo FDA UDI
Generic Name
General-purpose surgical microscope FDA UDI
Device Name
ARveo stand system for M530 microscope - for Leica surgical operating microscope system: ARveo FDA UDI
Model / Reference
000000000010448999 FDA UDI
Description
ARveo stand system for M530 microscope - for Leica surgical operating microscope system: ARveo FDA UDI

Identifiers

Catalog Number
10448999 FDA UDI
Primary DI / UDI-DI
07630003593280 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
Not 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

ARveo by Leica Microsystems (Schweiz) AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI 6dd63d00-03f8-4720-8dba-82c93ef72301 37 fields · synced Jun 1, 2026