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SiphonX® GRAVITATIONAL ANTI-SIPHON DEVICE

EUDAMEDFDA UDI

Class III (EU MDR)

Ref SX-200

by Sophysa

Identity

Trade Name
SiphonX® GRAVITATIONAL ANTI-SIPHON DEVICE EUDAMED
Sophysa FDA UDI
Generic Name
Cerebrospinal fluid shunt valve FDA UDI
Device Name
SiphonX® GRAVITATIONAL ANTI-SIPHON DEVICE EUDAMED
SIPHONX GRAVITATIONAL ANTI-SIPHON DEVICE FDA UDI
Model / Reference
SX-200 EUDAMEDFDA UDI
Description
SIPHONX GRAVITATIONAL ANTI-SIPHON DEVICE FDA UDI

Identifiers

Primary DI / UDI-DI
03760124131697 EUDAMEDFDA UDI
Basic UDI-DI
B-03760124131697 EUDAMED
510(k) Number
K091328 FDA UDI
FDA Product Code
JXG FDA UDI
EMDN Code
N01038099 INTRACRANIAL DRAINAGE DEVICES AND KITS - ACCESSORIES - OTHER 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
Greece 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

SiphonX® GRAVITATIONAL ANTI-SIPHON DEVICE by Sophysa — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sophysa
EUDAMED SRN
FR-MF-000002870

Sources (2)

  • EUDAMED 4a6dc50e-251e-47a7-9f79-477c90bdbdf7 61 fields · synced Jun 19, 2026
  • FDA UDI 84e41d84-4226-4427-bbab-2029ee2581e1 34 fields · synced May 30, 2026