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LASIK Cannulas

FDA UDI

Class I (US FDA UDI)

by Aurora Surgical, Llc

Identity

Trade Name
LASIK Cannulas FDA UDI
Generic Name
Ophthalmic angular gauge, reusable FDA UDI
Device Name
LASIK Interface Cannula, 25 Gauge With Spatulated Tip FDA UDI
Model / Reference
AS13-1702 FDA UDI
Description
LASIK Interface Cannula, 25 Gauge With Spatulated Tip FDA UDI

Identifiers

Catalog Number
AS13-1702 FDA UDI
Primary DI / UDI-DI
08175700111546 FDA UDI
FDA Product Code
HLF FDA UDI
GMDN Term
Ophthalmic angular gauge, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1430 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 angular gauge, reusable

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

Similar devices

Also classified as Ophthalmic angular gauge, 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 b5af305c-a761-4ac6-9064-c8c01e4566cc 35 fields · synced May 30, 2026