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Constellation

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
CONSTELLATION FDA UDI
Generic Name
Phacoemulsification/vitrectomy system generator FDA UDI
Device Name
CONSTELLATION BASE FDA UDI
Model / Reference
8065751451 FDA UDI
Description
CONSTELLATION BASE FDA UDI

Identifiers

Primary DI / UDI-DI
00380657514519 FDA UDI
FDA Product Code
HQE FDA UDI
HQC FDA UDI
GMDN Term
Phacoemulsification/vitrectomy system generator 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/vitrectomy system generator

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

Similar devices

Also classified as Phacoemulsification/vitrectomy system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (1)

  • FDA UDI 7fa0b15f-195f-4e4c-81b3-919e41677841 34 fields · synced May 30, 2026