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Fraxion Vacuum Pump

EUDAMEDFDA UDI

Class I (EU MDR)

Ref P10106-106

by 3C-Medical Intelligence GmbH

Identity

Trade Name
Fraxion Vacuum Pump EUDAMED
Fraxion FDA UDI
Generic Name
Stereotactic radiosurgical/radiotherapy arch head frame FDA UDI
Device Name
Fraxion EUDAMED
Fraxion™ Vacuum Pump provides vacuum to fix the Fraxion™ Mouthpiece and to evacuate the Fraxion™ Vacuum Cushion. FDA UDI
Model / Reference
P10106-106 EUDAMEDFDA UDI
Description
Fraxion™ Vacuum Pump provides vacuum to fix the Fraxion™ Mouthpiece and to evacuate the Fraxion™ Vacuum Cushion. FDA UDI

Identifiers

Catalog Number
P10106-106 FDA UDI
Primary DI / UDI-DI
04056719001575 EUDAMEDFDA UDI
Basic UDI-DI
04056719BUDI0000000002HW EUDAMED
Direct Marketing DI
04056719001575 EUDAMED
510(k) Number
K112210 FDA UDI
FDA Product Code
IYE FDA UDI
EMDN Code
V0804 PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures) EUDAMED
GMDN Term
Stereotactic radiosurgical/radiotherapy arch head frame FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Fraxion Vacuum Pump by 3C-Medical Intelligence GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000023763

Sources (2)

  • EUDAMED 2fc74daa-b4f4-4173-b686-ad4c69b99a95 61 fields · synced Jun 17, 2026
  • FDA UDI 3c85d67c-cf8b-4b86-ae00-67bcc6b661a2 36 fields · synced May 30, 2026