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Test Chambers for Irrigation/Aspiration Cannulas

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Test Chambers for Irrigation/Aspiration Cannulas FDA UDI
Generic Name
Ophthalmic cannulation set, reusable FDA UDI
Device Name
Test Chambers for Irrigation/Aspiration Cannulas FDA UDI
Model / Reference
16-3113 FDA UDI
Description
Test Chambers for Irrigation/Aspiration Cannulas FDA UDI

Identifiers

Primary DI / UDI-DI
00192896107847 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Ophthalmic cannulation set, 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 cannulation set, reusable

Test Chambers for Irrigation/Aspiration Cannulas by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic cannulation set, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f9b34051-78bd-4876-84d5-69bf65909734 34 fields · synced May 30, 2026