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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
Electrical-only medical device connection cable, reusable FDA UDI
Device Name
5 MM ASPIRATION/INJECTION NEEDLE, 16 GAUGE, 40 CM LENGTH FDA UDI
Model / Reference
CD950 FDA UDI
Description
5 MM ASPIRATION/INJECTION NEEDLE, 16 GAUGE, 40 CM LENGTH FDA UDI

Identifiers

Catalog Number
CD950 FDA UDI
Primary DI / UDI-DI
20653405043321 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Electrical-only medical device connection cable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical-only medical device connection cable, reusable

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

Similar devices

Also classified as Electrical-only medical device connection cable, 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 ea91e450-14e4-4fcc-aba4-4743c794097f 35 fields · synced May 31, 2026