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Monarch Advanced Imaging Accessory Kit

FDA UDI

Class II (US FDA UDI)

by Auris Health, Inc.

Identity

Trade Name
Monarch Advanced Imaging Accessory Kit FDA UDI
Generic Name
Robotic surgical arm system FDA UDI
Device Name
Window Field Generator, Connection Cable, Mounting System FDA UDI
Model / Reference
MON-000709 FDA UDI
Description
Window Field Generator, Connection Cable, Mounting System FDA UDI

Identifiers

Catalog Number
MON-000709 FDA UDI
Primary DI / UDI-DI
B634MON0007090 FDA UDI
510(k) Number
K211493 FDA UDI
FDA Product Code
EOQ FDA UDI
JAK FDA UDI
GMDN Term
Robotic surgical arm system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4680 FDA UDI
892.1750 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Robotic surgical arm system

Monarch Advanced Imaging Accessory Kit by Auris Health, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Robotic surgical arm system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Auris Health, Inc.

Sources (1)

  • FDA UDI e66064c2-93bf-4afd-9cfc-568c532fe6bd 35 fields · synced Jun 8, 2026