← Back to catalogue

McINTYRE LACRIMAL CANNULA

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
McINTYRE LACRIMAL CANNULA FDA UDI
Generic Name
Ophthalmic working-channel cannula, reusable FDA UDI
Device Name
McINTYRE LACRIMAL CANNULA CURVED TIP DUAL SIDEPORTS FDA UDI
Model / Reference
16-3330 FDA UDI
Description
McINTYRE LACRIMAL CANNULA CURVED TIP DUAL SIDEPORTS FDA UDI

Identifiers

Catalog Number
16-3330 FDA UDI
Primary DI / UDI-DI
00192896074897 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic working-channel cannula, 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 23 Gauge FDA UDI

Category: Ophthalmic working-channel cannula, reusable

McINTYRE LACRIMAL CANNULA by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic working-channel cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI f22b08a7-d214-4ef7-959c-7441fa500953 36 fields · synced May 30, 2026