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Infiniti

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
Infiniti FDA UDI
Generic Name
Phacoemulsification system handpiece FDA UDI
Device Name
Ultrasonic Handpiece FDA UDI
Model / Reference
8065750121 FDA UDI
Description
Ultrasonic Handpiece FDA UDI

Identifiers

Primary DI / UDI-DI
00380657501212 FDA UDI
FDA Product Code
HQC FDA UDI
HQE FDA UDI
GMDN Term
Phacoemulsification system handpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4670 FDA UDI
886.4150 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Phacoemulsification system handpiece

Infiniti by Alcon Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phacoemulsification system handpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01aebed9-c0d3-4271-a24b-de95b991d1fe 34 fields · synced Jun 8, 2026