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Heartline Cooley Scissors

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
HEARTLINE COOLEY SCISSORS FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI
Device Name
HEARTLINE COOLEY SCISSORS CURVED TUNGSTEN CARBIDE BLADE SQUEEZE HANDLE FDA UDI
Model / Reference
2800-246S FDA UDI
Description
HEARTLINE COOLEY SCISSORS CURVED TUNGSTEN CARBIDE BLADE SQUEEZE HANDLE FDA UDI

Identifiers

Catalog Number
2800-246S FDA UDI
Primary DI / UDI-DI
00192896075573 FDA UDI
510(k) Number
K152400 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, reusable

Heartline Cooley Scissors by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, reusable.

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 1715d12a-cd25-4858-adb9-39df4ec8276a 37 fields · synced May 30, 2026