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Amo Test Chamber

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
AMO TEST CHAMBER FDA UDI
Generic Name
Ophthalmic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
PHACO TEST CHAMBER, REUSABLE, STERILE FDA UDI
Model / Reference
OM3452022 FDA UDI
Description
PHACO TEST CHAMBER, REUSABLE, STERILE FDA UDI

Identifiers

Catalog Number
OM3452022 FDA UDI
Primary DI / UDI-DI
05050474520769 FDA UDI
FDA Product Code
HQC FDA UDI
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, reusable 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic surgical procedure kit, non-medicated, reusable

Amo Test Chamber by Johnson & Johnson Surgical Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Johnson & Johnson Surgical Vision, Inc.

Sources (1)

  • FDA UDI 021da617-4157-455b-881c-fe883342ce17 35 fields · synced Jun 9, 2026