Clearview®

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name: CLEARVIEW® FDA UDI
Generic Name: Surgical mist irrigation tip FDA UDI
Device Name: BLOWER/MISTER KIT 22120 CLEARVIEW 10P 15 FDA UDI
Model / Reference: 22120 FDA UDI
Description: BLOWER/MISTER KIT 22120 CLEARVIEW 10P 15 FDA UDI

Identifiers

Primary DI / UDI-DI: 20643169423170 FDA UDI
FDA Product Code: FQH FDA UDI
GMDN Term: Surgical mist irrigation tip FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5475 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical mist irrigation tip

Clearview® by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medtronic, Inc.

Sources (1)

FDA UDI 41a7e3ee-a47a-4d50-a67a-9d227d389867 34 fields · synced Jun 8, 2026