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Kirwan

FDA UDI

Class II (US FDA UDI)

by Kirwan Surgical Products Llc

Identity

Trade Name
Kirwan FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
4" Disposable Jewelers/Iris Non-Stick Bipolar Forceps, Straight, 0.4mm Tip, Blue Insulation, Geuder Logo (Special) FDA UDI
Model / Reference
14-3000S FDA UDI
Description
4" Disposable Jewelers/Iris Non-Stick Bipolar Forceps, Straight, 0.4mm Tip, Blue Insulation, Geuder Logo (Special) FDA UDI

Identifiers

Primary DI / UDI-DI
00841019116043 FDA UDI
510(k) Number
K900533 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

FDA UDI
Sterilization Method
Radiation Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 4 Inch FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Kirwan by Kirwan Surgical Products Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical handpiece/electrode, bipolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a2bd8fbf-43fd-4a4c-933b-5343f1321233 36 fields · synced May 30, 2026