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Core Dynamics

FDA UDI

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CORE DYNAMICS FDA UDI
Generic Name
Laparoscopic trocar blade, single-use FDA UDI
Device Name
10mm Gasket, Replacement Part, Reusable FDA UDI
Model / Reference
CD4GKM FDA UDI
Description
10mm Gasket, Replacement Part, Reusable FDA UDI

Identifiers

Catalog Number
CD4GKM FDA UDI
Primary DI / UDI-DI
20653405045752 FDA UDI
510(k) Number
K950457 FDA UDI
FDA Product Code
FBM FDA UDI
GMDN Term
Laparoscopic trocar blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5090 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

Yes

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

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 4ba235ce-e87b-452b-a001-36bf94de0d4e 38 fields · synced May 30, 2026