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Codman

FDA UDI

Class II (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
CODMAN FDA UDI
Generic Name
Intracerebral trocar blade FDA UDI
Device Name
CODMAN Disposable Split Trocar FDA UDI
Model / Reference
82-4095 FDA UDI
Description
CODMAN Disposable Split Trocar FDA UDI

Identifiers

Catalog Number
824095 FDA UDI
Primary DI / UDI-DI
10886704041948 FDA UDI
510(k) Number
K973774 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Intracerebral trocar blade FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Codman by Cerenovus, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K973774 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cerenovus, Inc.

Sources (1)

  • FDA UDI e5fe116a-0db3-4be8-9805-931706a5231f 37 fields · synced Jun 1, 2026