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CODMAN CERTAS® Plus

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Switzerland Sàrl

Identity

Trade Name
CODMAN CERTAS® Plus FDA UDI
Generic Name
Ventriculo-peritoneal/atrial shunt FDA UDI
Device Name
CODMAN CERTAS® Plus Programable Valve Inline Valve Only with SIPHONGUARD® Includes: Priming Adapter and Information Manual FDA UDI
Model / Reference
828804PL FDA UDI
Description
CODMAN CERTAS® Plus Programable Valve Inline Valve Only with SIPHONGUARD® Includes: Priming Adapter and Information Manual FDA UDI

Identifiers

Catalog Number
82-8804PL FDA UDI
Primary DI / UDI-DI
10381780521174 FDA UDI
FDA Product Code
JXG FDA UDI
GMDN Term
Ventriculo-peritoneal/atrial shunt FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 FDA UDI
Commercial Distribution
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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Ventriculo-peritoneal/atrial shunt

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

Similar devices

Also classified as Ventriculo-peritoneal/atrial shunt.

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 ce52277c-ecf3-4a42-bba3-eb36b01efce2 36 fields · synced May 30, 2026