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 Only Includes: Priming Adapter and Information Manual FDA UDI
Model / Reference: 828820PL FDA UDI
Description: CODMAN CERTAS® Plus Programmable Valve Right Angle Valve Only Includes: Priming Adapter and Information Manual FDA UDI

Identifiers

Catalog Number: 82-8820PL FDA UDI
Primary DI / UDI-DI: 10381780529439 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Integra LifeSciences Switzerland Sàrl

Sources (1)

FDA UDI 7fd5932d-1c2a-443d-8963-2b93de7de8be 36 fields · synced Jun 6, 2026