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Codman Icp Express

FDA UDI

Class II (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
CODMAN ICP EXPRESS FDA UDI
Generic Name
Intracranial pressure monitor FDA UDI
Device Name
Power Supply 120/127 VAC 50-60HZ FDA UDI
Model / Reference
82-6634 FDA UDI
Description
Power Supply 120/127 VAC 50-60HZ FDA UDI

Identifiers

Catalog Number
826634 FDA UDI
Primary DI / UDI-DI
10886704042341 FDA UDI
510(k) Number
K945585 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
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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Cleared under the same submission

K945585 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 97074d62-cf12-4267-8619-f919051c0f44 38 fields · synced May 31, 2026