Centurion

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name: Centurion FDA UDI
Generic Name: Phacoemulsification system FDA UDI
Device Name: Centurion Vision System With Active Sentry without IV Pole FDA UDI
Model / Reference: 8065000565 FDA UDI
Description: Centurion Vision System With Active Sentry without IV Pole FDA UDI

Identifiers

Primary DI / UDI-DI: 00380650005656 FDA UDI
FDA Product Code: HQC FDA UDI
GMDN Term: Phacoemulsification system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4670 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Phacoemulsification system

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

Similar devices

Also classified as Phacoemulsification system.

WHITESTAR SIGNATURE — Johnson & Johnson Surgical Vision, Inc. · Class II
WHITESTAR SIGNATURE — Johnson & Johnson Surgical Vision, Inc. · Class II
WHITESTAR TECHNOLOGY — Johnson & Johnson Surgical Vision, Inc. · Class II
UNIVERSAL IV POLE EXTENDER — Johnson & Johnson Surgical Vision, Inc. · Class II
WHITESTAR SIGNATURE — Johnson & Johnson Surgical Vision, Inc. · Class II
WHITESTAR PHACO HANDPIECE — Johnson & Johnson Surgical Vision, Inc. · Class II
WHITESTAR SIGNATURE PRO — Johnson & Johnson Surgical Vision, Inc. · Class II
SOVEREIGN COMPACT — Johnson & Johnson Surgical Vision, Inc. · Class II

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: Alcon Laboratories, Inc.

Sources (1)

FDA UDI 502c119a-669d-480f-922f-71a3fb66f866 33 fields · synced Jun 1, 2026