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Ring Cannula

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Ring Cannula FDA UDI
Generic Name
Ophthalmic working-channel cannula, reusable FDA UDI
Device Name
Ring Cannula 2 Side Ports 1/3 Turn Separation 1 Millimeter Down 24 Gauge FDA UDI
Model / Reference
16-3990 FDA UDI
Description
Ring Cannula 2 Side Ports 1/3 Turn Separation 1 Millimeter Down 24 Gauge FDA UDI

Identifiers

Primary DI / UDI-DI
00192896107854 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

Category: Ophthalmic working-channel cannula, reusable

Ring 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

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Manufacturer

Manufacturer
Sontec Instruments, Inc.

Sources (1)

  • FDA UDI d4434b9e-60d8-4111-93e0-3bd4a770b465 34 fields · synced May 30, 2026