← Back to catalogue

VacQfix™

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref RT-4517-100100TRAPF35MModel Vacuum Cushions

by Qfix

Identity

Trade Name
VacQfix™ FDA UDI
Generic Name
Vacuum-mould patient positioning system FDA UDI
Device Name
VacQfix Cushion, 100cm x 100cm, TRAP 35L fill FDA UDI
Model / Reference
RT-4517-100100TRAPF35M EUDAMEDFDA UDI
Vacuum Cushions EUDAMED
Description
VacQfix Cushion, 100cm x 100cm, TRAP 35L fill FDA UDI

Identifiers

Catalog Number
RT-4517-100100TRAPF35M FDA UDI
Primary DI / UDI-DI
10841962118849 EUDAMEDFDA UDI
Basic UDI-DI
8419621VACQFIX5A EUDAMED
FDA Product Code
JAI FDA UDI
EMDN Code
Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
GMDN Term
Vacuum-mould patient positioning system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.5770 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
Width — 70 Centimeter FDA UDI
Length — 100 Centimeter FDA UDI
Width — 100 Centimeter FDA UDI
Total Volume — 35 Liter FDA UDI

Category: Vacuum-mould patient positioning system

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

Similar devices

Also classified as Vacuum-mould patient positioning system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Qfix

Sources (2)

  • FDA UDI bbb31902-ae55-4146-bec3-9f0912e0009b 36 fields · synced Jun 18, 2026
  • EUDAMED 5ee93587-68c7-4444-bd46-cc915dda9ade 61 fields · synced Jun 18, 2026