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Codman Certas Siphonguard

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
CODMAN CERTAS SIPHONGUARD FDA UDI
Generic Name
Ventriculo-peritoneal/atrial shunt FDA UDI
Device Name
CODMAN CERTAS SIPHONGUARD Plus Programmable Valve Inline Small Valve with SIPHONGUARD, Accessories and Unitized Catheter Includes: Ventricular Catheter, Unitized Distal Catheter, Priming Adapter, Right Angle Adapter and Information Manual FDA UDI
Model / Reference
82-8816PL FDA UDI
Description
CODMAN CERTAS SIPHONGUARD Plus Programmable Valve Inline Small Valve with SIPHONGUARD, Accessories and Unitized Catheter Includes: Ventricular Catheter, Unitized Distal Catheter, Priming Adapter, Right Angle Adapter and Information Manual FDA UDI

Identifiers

Catalog Number
828816PL FDA UDI
Primary DI / UDI-DI
10886704081951 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
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
MRI Safety
MR Conditional FDA UDI

Codman Certas Siphonguard by Medos International Sàrl — 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
Medos International Sàrl

Sources (1)

  • FDA UDI eae45c6f-9a94-4fd0-b59e-ea99a3c2c5e7 36 fields · synced Jun 1, 2026