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Olympus

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
Olympus FDA UDI
Generic Name
Operating room equipment remote control FDA UDI
Device Name
ES-IP BASE SYSTEM, SPLIT RACK, FREESTANDING OPTION with Optional Equipment FDA UDI
Model / Reference
ISM-1200305 FDA UDI
Description
ES-IP BASE SYSTEM, SPLIT RACK, FREESTANDING OPTION with Optional Equipment FDA UDI

Identifiers

Primary DI / UDI-DI
00810008185162 FDA UDI
FDA Product Code
FTA FDA UDI
GMDN Term
Operating room equipment remote control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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

Yes

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

No

FDA UDI

Category: Operating room equipment remote control

Olympus by Gyrus Acmi, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room equipment remote control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gyrus Acmi, Inc.

Sources (1)

  • FDA UDI 3bdc2039-1ad5-4c98-8ecc-1a07b14b5b78 33 fields · synced May 31, 2026