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USA Elite

FDA UDI

Class II (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
USA Elite FDA UDI
Generic Name
Rigid optical cystourethroscope FDA UDI
Device Name
USA Elite System Cystourethroscope Short Bridge, Double-Horn FDA UDI
Model / Reference
E153 FDA UDI
Description
USA Elite System Cystourethroscope Short Bridge, Double-Horn FDA UDI

Identifiers

Primary DI / UDI-DI
00821925003262 FDA UDI
510(k) Number
K890328 FDA UDI
FDA Product Code
HIH FDA UDI
GMDN Term
Rigid optical cystourethroscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1690 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical cystourethroscope

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

Similar devices

Also classified as Rigid optical cystourethroscope.

Cleared under the same submission

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 a2a8cb80-c56c-4033-aa6a-91be7d809392 34 fields · synced May 30, 2026