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Gyrus Acmi

FDA UDI

Class I (US FDA UDI)

by Gyrus Acmi, Inc.

Identity

Trade Name
GYRUS ACMI FDA UDI
Generic Name
Paranasal sinus irrigation/aspiration cannula FDA UDI
Device Name
DISPOSABLE RAINS SINUS IRRIGATION CANNULA, MALLEABLE SHAFT WORKING LENGTH: 4.25" (108MM) DIAMETER: 6 FRENCH FDA UDI
Model / Reference
70131011 FDA UDI
Description
DISPOSABLE RAINS SINUS IRRIGATION CANNULA, MALLEABLE SHAFT WORKING LENGTH: 4.25" (108MM) DIAMETER: 6 FRENCH FDA UDI

Identifiers

Primary DI / UDI-DI
00821925040397 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Paranasal sinus irrigation/aspiration cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Paranasal sinus irrigation/aspiration cannula

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

Similar devices

Also classified as Paranasal sinus irrigation/aspiration cannula.

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 f4dccad9-c0e8-4321-b9ad-b313cac2768c 33 fields · synced Jun 1, 2026