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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
15mm x 60mm Thoracoscopy Cannula With Blunt Tip Trocar, Reusable FDA UDI
Model / Reference
CD1415 FDA UDI
Description
15mm x 60mm Thoracoscopy Cannula With Blunt Tip Trocar, Reusable FDA UDI

Identifiers

Catalog Number
CD1415 FDA UDI
Primary DI / UDI-DI
20653405044779 FDA UDI
510(k) Number
K932022 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI d1458c31-9ca0-4d16-838d-fba3090adf2b 38 fields · synced May 31, 2026