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Millennium

FDA UDI

Class II (US FDA UDI)

by Bausch & Lomb Incorporated

Identity

Trade Name
Millennium FDA UDI
Generic Name
Phacoemulsification system handpiece FDA UDI
Device Name
Millennium Phaco Handpice FDA UDI
Model / Reference
CX7000 FDA UDI
Description
Millennium Phaco Handpice FDA UDI

Identifiers

Catalog Number
CX7000 FDA UDI
Primary DI / UDI-DI
00757770454099 FDA UDI
FDA Product Code
HQE FDA UDI
HQC FDA UDI
GMDN Term
Phacoemulsification system handpiece FDA UDI

Classification

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

Category: Phacoemulsification system handpiece

Millennium by Bausch & Lomb Incorporated — 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 261c7726-7b5c-40fe-ba35-13adaa133117 34 fields · synced Jun 8, 2026