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Amo Tac Infusion Sleeve

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name
AMO TAC INFUSION SLEEVE FDA UDI
Generic Name
Vitrectomy system handpiece FDA UDI
Device Name
PARTS LIST, INFUSION SLEEVE ASEMBLY FDA UDI
Model / Reference
OM0527011 FDA UDI
Description
PARTS LIST, INFUSION SLEEVE ASEMBLY FDA UDI

Identifiers

Catalog Number
OM0527011 FDA UDI
Primary DI / UDI-DI
05050474520509 FDA UDI
FDA Product Code
HKP FDA UDI
GMDN Term
Vitrectomy system handpiece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vitrectomy system handpiece

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

Similar devices

Also classified as Vitrectomy system handpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4df08633-375f-4f97-81ac-7d2951d3d6a5 35 fields · synced Jun 9, 2026