Disposable 25ga Vitrectomy Cutter

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name: DISPOSABLE 25GA VITRECTOMY CUTTER FDA UDI
Generic Name: Vitrectomy system handpiece FDA UDI
Device Name: DISPOSABLE 25GA VITRECTOMY CUTTER FDA UDI
Model / Reference: NGP0025 FDA UDI
Description: DISPOSABLE 25GA VITRECTOMY CUTTER FDA UDI

Identifiers

Catalog Number: NGP0025 FDA UDI
Primary DI / UDI-DI: 05050474534117 FDA UDI
FDA Product Code: MLZ 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Vitrectomy system handpiece

Disposable 25ga Vitrectomy Cutter 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.

Constellation, EDGE PLUS, TOTAL PLUS, ULTRAVIT — Alcon Laboratories, Inc. · Class II
Constellation — Alcon Laboratories, Inc. · Class II
Constellation, EDGE PLUS, TOTAL PLUS, ULTRAVIT — Alcon Laboratories, Inc. · Class II
CONSTELLATION® ULTRAVIT® ENGAUGE® — Alcon Laboratories, Inc. · Class II
Constellation, Ultravit, TotalPlus, Engauge — Alcon Laboratories, Inc. · Class II
Engauge — Alcon Laboratories, Inc. · Class II
Constellation, EDGE PLUS, TOTAL PLUS, ULTRAVIT — Alcon Laboratories, Inc. · Class II
27+® Infusion Cannula w/Tray — Alcon Laboratories, Inc. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Johnson & Johnson Surgical Vision, Inc.

Sources (1)

FDA UDI a1bcaf78-dcfa-4bf9-bf51-bf2d2cfb026a 35 fields · synced Jun 9, 2026