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Codman Hakim Rickham Siphonguard

FDA UDI

Class II (US FDA UDI)

by Cerenovus, Inc.

Identity

Trade Name
CODMAN HAKIM RICKHAM SIPHONGUARD FDA UDI
Generic Name
Cerebrospinal fluid shunt valve FDA UDI
Device Name
CODMAN HAKIM Programmable Valve with Unitized RICKHAM Reservoir and Unitized SIPHONGUARD Device Programmable in steps of 10mm H2O (98Pa): 30mm H2O to 200mm H2O (294Pa-1960Pa) Includes: Priming Adapter and Information Manual FDA UDI
Model / Reference
NS5053 FDA UDI
Description
CODMAN HAKIM Programmable Valve with Unitized RICKHAM Reservoir and Unitized SIPHONGUARD Device Programmable in steps of 10mm H2O (98Pa): 30mm H2O to 200mm H2O (294Pa-1960Pa) Includes: Priming Adapter and Information Manual FDA UDI

Identifiers

Catalog Number
NS5053 FDA UDI
Primary DI / UDI-DI
10886704046769 FDA UDI
510(k) Number
K020667 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Cerebrospinal fluid shunt valve 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

Yes

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
MRI Safety
MR Conditional FDA UDI

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

Cleared under the same submission

K020667 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 f77ce3f3-0098-4579-9506-563fc7a2c090 37 fields · synced May 30, 2026