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VIA360 Surgical System

FDA UDI

Class II (US FDA UDI)

by New World Medical, Incorporated

Identity

Trade Name
VIA360 Surgical System FDA UDI
Generic Name
Ophthalmic knife, single-use FDA UDI
Device Name
VIA360 Surgical System FDA UDI
Model / Reference
VIA360 FDA UDI
Description
VIA360 Surgical System FDA UDI

Identifiers

Catalog Number
10-0615 FDA UDI
Primary DI / UDI-DI
00892064002362 FDA UDI
510(k) Number
K243503 FDA UDI
FDA Product Code
MRH FDA UDI
HMZ FDA UDI
GMDN Term
Ophthalmic knife, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 FDA UDI
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic knife, single-useOphthalmic surgical irrigation/infusion/aspiration handle, single-use

VIA360 Surgical System by New World Medical, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical irrigation/infusion/aspiration handle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
New World Medical, Incorporated

Sources (1)

  • FDA UDI 247b39d7-2bdd-4839-b6a1-8235da530fe5 36 fields · synced May 31, 2026