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Core Dynamics

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CORE DYNAMICS FDA UDI
Generic Name
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
10/12mm Open Lapsrosoopilc Adapter and Blunt Tip Trocar for Entree Plus and Entree II Cannula, Reusable FDA UDI
Model / Reference
CD1406 FDA UDI
Description
10/12mm Open Lapsrosoopilc Adapter and Blunt Tip Trocar for Entree Plus and Entree II Cannula, Reusable FDA UDI

Identifiers

Catalog Number
CD1406 FDA UDI
Primary DI / UDI-DI
20653405044700 FDA UDI
510(k) Number
K932020 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic surgical procedure kit, non-medicated, reusable

Core Dynamics by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI c2637544-23f6-4bd1-8e3a-a49efbdbca41 37 fields · synced May 30, 2026