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Disposable Bipolar Forceps, 8”, 1.0mm Curved Up Tips

FDA UDI

Class II (US FDA UDI)

by Katalyst Surgical, Llc

Identity

Trade Name
Disposable Bipolar Forceps, 8”, 1.0mm Curved Up Tips FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
Box, International, Disposable Bipolar Forceps, 8", 1.0mm FDA UDI
Model / Reference
DNK8-10U FDA UDI
Description
Box, International, Disposable Bipolar Forceps, 8", 1.0mm FDA UDI

Identifiers

Primary DI / UDI-DI
00856312006281 FDA UDI
510(k) Number
K123172 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
Not 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

No

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

Disposable Bipolar Forceps, 8”, 1.0mm Curved Up Tips by Katalyst Surgical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K123172 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 d21267b4-ccbe-4335-8c4c-287fd2b91ec9 35 fields · synced May 30, 2026