ClearCut® +1 more model

FDA UDI

Class I (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name: ClearCut®; Intrepid FDA UDI
Generic Name: Ophthalmic knife, single-use FDA UDI
Device Name: ClearCut® S Intrepid Micro-coaxial system Safety Slit Knife 2.2 DB FDA UDI
Model / Reference: 8065772265 FDA UDI
Description: ClearCut® S Intrepid Micro-coaxial system Safety Slit Knife 2.2 DB FDA UDI

Identifiers

Primary DI / UDI-DI: 00380657722655 FDA UDI
FDA Product Code: HNN FDA UDI
GMDN Term: Ophthalmic knife, single-use FDA UDI
Models / Variants: ClearCut® FDA UDI
Intrepid FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic knife, single-use

ClearCut® +1 more model by Alcon Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — 2 models — 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 I	Pending data

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Manufacturer

Manufacturer: Alcon Laboratories, Inc.

Sources (1)

FDA UDI fda67316-e9a1-4ac5-a2e6-a6688f65087f 34 fields · synced May 31, 2026