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Cannulas

FDA UDI

Class I (US FDA UDI)

by Aurora Surgical, Llc

Identity

Trade Name
Cannulas FDA UDI
Generic Name
Ophthalmic surgical irrigation/infusion/aspiration handle, reusable FDA UDI
Device Name
Microsurgical Handle, Female-Female, Titanium, Overall Length 80mm FDA UDI
Model / Reference
AS13-1902T FDA UDI
Description
Microsurgical Handle, Female-Female, Titanium, Overall Length 80mm FDA UDI

Identifiers

Catalog Number
AS13-1902T FDA UDI
Primary DI / UDI-DI
08175700155120 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic surgical irrigation/infusion/aspiration handle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ophthalmic surgical irrigation/infusion/aspiration handle, reusable

Cannulas by Aurora Surgical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical irrigation/infusion/aspiration handle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aurora Surgical, Llc

Sources (1)

  • FDA UDI 574c0d7b-046c-4883-a00f-572a2d84731b 34 fields · synced May 30, 2026