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Codman® Hakim®

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 82-3007

by Integra LifeSciences Production Corporation

Identity

Trade Name
CODMAN® HAKIM® EUDAMEDFDA UDI
Generic Name
Cerebrospinal fluid shunt valve FDA UDI
Device Name
Hakim Precision Valve EUDAMED
Precision Fixed Pressure Valve Cylindrical Valve with Prechamber and Unitized Distal Catheter Low Range FDA UDI
Model / Reference
82-3007 EUDAMED
823007 FDA UDI
Description
Precision Fixed Pressure Valve Cylindrical Valve with Prechamber and Unitized Distal Catheter Low Range FDA UDI

Identifiers

Catalog Number
82-3007 FDA UDI
Primary DI / UDI-DI
10381780534068 EUDAMEDFDA UDI
Basic UDI-DI
B-10381780534068 EUDAMED
510(k) Number
K221840 FDA UDI
FDA Product Code
JXG FDA UDI
EMDN Code
N010301 VENTRICULAR-PERITONEAL SHUNTS EUDAMED
GMDN Term
Cerebrospinal fluid shunt valve FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
882.5550 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cerebrospinal fluid shunt valve

Codman® Hakim® by Integra LifeSciences Production Corporation — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cerebrospinal fluid shunt valve.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI f99610c3-cb12-487c-9ac4-e472acf51d56 37 fields · synced Oct 8, 2026
  • EUDAMED 9acf05ea-83cc-4341-a9ed-0b19d0024ade 61 fields · synced Oct 7, 2026