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Suction Tube

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
Suction Tube FDA UDI
Generic Name
Surgical irrigation/aspiration cannula, illuminating, reusable FDA UDI
Device Name
Yankauer Suction Tube With Universal Fiber Optic Light Guide FDA UDI
Model / Reference
180-449 FDA UDI
Description
Yankauer Suction Tube With Universal Fiber Optic Light Guide FDA UDI

Identifiers

Primary DI / UDI-DI
00192896103573 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical irrigation/aspiration cannula, illuminating, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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
Length — 11.25 Inch FDA UDI

Category: Surgical irrigation/aspiration cannula, illuminating, reusable

Suction Tube by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration cannula, illuminating, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55ae1089-6258-4292-b824-c6ab242bd73c 35 fields · synced Jun 8, 2026