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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 Programmable Valve Right Angle Valve with Accessories and Unitised BACTISEAL® Catheter FDA UDI
Model / Reference
828823PL FDA UDI
Description
CODMAN® CERTAS® Plus Programmable Valve Right Angle Valve with Accessories and Unitised BACTISEAL® Catheter FDA UDI

Identifiers

Catalog Number
82-8823PL FDA UDI
Primary DI / UDI-DI
10381780529279 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

No

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 88acac33-d500-48d9-89c3-56973084a762 36 fields · synced May 29, 2026