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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
Ventriculoperitoneal shunt FDA UDI
Device Name
CODMAN HAKIM Precision Fixed Pressure Valve MICRO II With SALMON-RICKHAM Reservoir and SIPHONGUARD Device Operating Pressure: 40mm H2O Plus or Minus 10mm H2O (392 Pa Plus or Minus 98 Pa) Low Range Includes: Ventricular Catheter 14cm, Stylet, Nonunitized Peritoneal Catheter 120cm, Priming Adapter and Information Manual FDA UDI
Model / Reference
NS0597 FDA UDI
Description
CODMAN HAKIM Precision Fixed Pressure Valve MICRO II With SALMON-RICKHAM Reservoir and SIPHONGUARD Device Operating Pressure: 40mm H2O Plus or Minus 10mm H2O (392 Pa Plus or Minus 98 Pa) Low Range Includes: Ventricular Catheter 14cm, Stylet, Nonunitized Peritoneal Catheter 120cm, Priming Adapter and Information Manual FDA UDI

Identifiers

Catalog Number
NS0597 FDA UDI
Primary DI / UDI-DI
10886704046011 FDA UDI
510(k) Number
K091346 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Ventriculoperitoneal shunt 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cerenovus, Inc.

Sources (1)

  • FDA UDI 064c976b-e7f4-473d-a9e0-7056ead2636d 37 fields · synced May 31, 2026