Core Dynamics

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: CORE DYNAMICS FDA UDI
Generic Name: Insufflation gas conditioning tubing set FDA UDI
Device Name: Insufflation Tubing With Luer Lock Connectors, 10 Foot length FDA UDI
Model / Reference: CD3000 FDA UDI
Description: Insufflation Tubing With Luer Lock Connectors, 10 Foot length FDA UDI

Identifiers

Catalog Number: CD3000 FDA UDI
Primary DI / UDI-DI: 10653405045465 FDA UDI
FDA Product Code: HES FDA UDI
GMDN Term: Insufflation gas conditioning tubing set FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.1300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Dimensions & Sizes

Size: Length — 3 Meter FDA UDI
Length — 10 Feet FDA UDI

Category: Insufflation gas conditioning tubing set

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Conmed Corporation

Sources (1)

FDA UDI 82359d79-58a2-423f-b15c-3c1aa7752c48 36 fields · synced May 30, 2026