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Codman®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Switzerland Sàrl

Identity

Trade Name
CODMAN® FDA UDI
Generic Name
Intracranial pressure monitor FDA UDI
Device Name
CODMAN® Patient Monitor Interface Cable - Fukuda Denshi (DS-8000) FDA UDI
Model / Reference
826888 FDA UDI
Description
CODMAN® Patient Monitor Interface Cable - Fukuda Denshi (DS-8000) FDA UDI

Identifiers

Catalog Number
82-6888 FDA UDI
Primary DI / UDI-DI
10381780520795 FDA UDI
510(k) Number
K152670 FDA UDI
FDA Product Code
GWM FDA UDI
GMDN Term
Intracranial pressure monitor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1620 FDA UDI
Commercial Distribution
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
MRI Safety
MR Unsafe FDA UDI

Category: Intracranial pressure monitor

Codman® by Integra LifeSciences Switzerland Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intracranial pressure monitor.

Cleared under the same submission

K152670 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integra LifeSciences Switzerland Sàrl

Sources (1)

  • FDA UDI 2a4a6e5f-09e2-4d30-a1b2-acb484ce3606 37 fields · synced Jun 1, 2026