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ZiFix Traverse

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref RT-4558CB04Model Stereotactic Body Radiation Therapy (SBRT)

by Medtec LLC

Identity

Trade Name
ZiFix Traverse FDA UDI
Generic Name
Radiological whole-body positioner FDA UDI
Device Name
ZiFix Traverse with ONEClamp FDA UDI
Model / Reference
RT-4558CB04 EUDAMEDFDA UDI
Stereotactic Body Radiation Therapy (SBRT) EUDAMED
Description
ZiFix Traverse with ONEClamp FDA UDI

Identifiers

Catalog Number
RT-4558CB04 FDA UDI
Primary DI / UDI-DI
00841439114841 EUDAMEDFDA UDI
Basic UDI-DI
8414391OC0017R01BH EUDAMED
510(k) Number
K171133 FDA UDI
FDA Product Code
IYE FDA UDI
JAI FDA UDI
JAK FDA UDI
KPS FDA UDI
LHN FDA UDI
LNH FDA UDI
OUO FDA UDI
EMDN Code
Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
GMDN Term
Radiological whole-body positioner FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
892.5770 FDA UDI
892.1750 FDA UDI
892.1200 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

Category: Radiological whole-body positioner

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

Similar devices

Also classified as Radiological whole-body positioner.

Cleared under the same submission

K171133 also covers:

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (2)

  • FDA UDI 2f16fae1-bd4f-461a-8ca2-dd8943f5399b 36 fields · synced Jun 20, 2026
  • EUDAMED 3133f1cf-1e4b-4912-ad43-03cf293d085f 61 fields · synced Jun 20, 2026