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ZiFix Traverse™

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref RT-4558CB03Model Breast and Pelvis

by Qfix

Identity

Trade Name
ZiFix Traverse™ FDA UDI
Generic Name
Indexed-immobilization patient positioning system FDA UDI
Device Name
ZiFix Traverse™ Abdominal/Thoracic Motion Control System FDA UDI
Model / Reference
RT-4558CB03 EUDAMEDFDA UDI
Breast and Pelvis EUDAMED
Description
ZiFix Traverse™ Abdominal/Thoracic Motion Control System FDA UDI

Identifiers

Catalog Number
RT-4558CB03 FDA UDI
Primary DI / UDI-DI
10841962111123 EUDAMEDFDA UDI
Basic UDI-DI
8419621BREASTPELVISTG EUDAMED
FDA Product Code
OUO FDA UDI
JAK FDA UDI
KPS FDA UDI
JAI FDA UDI
LHN FDA UDI
LNH FDA UDI
IYE FDA UDI
EMDN Code
Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
GMDN Term
Indexed-immobilization patient positioning system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.1200 FDA UDI
892.1750 FDA UDI
892.5770 FDA UDI
892.5050 FDA UDI
892.1000 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 130 Centimeter FDA UDI
Width — 13 Centimeter FDA UDI
Length — 170 Centimeter FDA UDI

Category: Indexed-immobilization patient positioning system

ZiFix Traverse™ by Qfix — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Indexed-immobilization patient positioning system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qfix

Sources (2)

  • FDA UDI feb2aa25-daf9-4138-9c30-e63152458d79 36 fields · synced Jun 19, 2026
  • EUDAMED 4570c6d5-9e7b-497e-9246-bc8ba96c8db6 61 fields · synced Jun 19, 2026