Sovereign Compact

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name: SOVEREIGN COMPACT FDA UDI
Generic Name: Phacoemulsification system FDA UDI
Device Name: SOVEREIGN CMPACT DC POWERED IV POLE FDA UDI
Model / Reference: CMP680P2 FDA UDI
Description: SOVEREIGN CMPACT DC POWERED IV POLE FDA UDI

Identifiers

Catalog Number: CMP680P2 FDA UDI
Primary DI / UDI-DI: 05050474514751 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

FDA UDI

Category: Phacoemulsification system

Sovereign Compact by Johnson & Johnson Surgical Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — 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 II	Pending data

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Manufacturer

Manufacturer: Johnson & Johnson Surgical Vision, Inc.

Sources (1)

FDA UDI e86a30ad-282b-4818-b84d-c4bd2922b3b3 35 fields · synced Jun 9, 2026