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Spetzler™ Lighted Suction Tube, 9 French, 120mm long

FDA UDI

Class II (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Spetzler™ Lighted Suction Tube, 9 French, 120mm long FDA UDI
Generic Name
Surgical/emergency suction cannula, illuminating, single-use FDA UDI
Device Name
Spetzler™ Lighted Suction Tube, 9 French, 120mm long, box of 5 FDA UDI
Model / Reference
DN1509-120 FDA UDI
Description
Spetzler™ Lighted Suction Tube, 9 French, 120mm long, box of 5 FDA UDI

Identifiers

Primary DI / UDI-DI
10817489025038 FDA UDI
510(k) Number
K141781 FDA UDI
FDA Product Code
FST FDA UDI
GMDN Term
Surgical/emergency suction cannula, illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/emergency suction cannula, illuminating, single-use

Spetzler™ Lighted Suction Tube, 9 French, 120mm long by Katalyst Surgical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, illuminating, single-use.

Cleared under the same submission

K141781 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Katalyst Surgical, Llc

Sources (1)

  • FDA UDI 5c64136e-4a3f-4771-8e09-4904f6b7c0ce 34 fields · synced May 30, 2026