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Fibreplast® Variable Perf™ Assure™ Open View with Integrated Shim™

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref RT-A892KYSDFModel Aquaplast RT and Fibreplast

by Qfix

Identity

Trade Name
Fibreplast® Variable Perf™ Assure™ Open View with Integrated Shim™ FDA UDI
Generic Name
Patient positioning thermoplastic mould material FDA UDI
Device Name
Fibreplast Open View Hd+Shldr S-Frame 3.2mm Variable Perf w/ Integrated Shim FDA UDI
Model / Reference
RT-A892KYSDF EUDAMEDFDA UDI
Aquaplast RT and Fibreplast EUDAMED
Description
Fibreplast Open View Hd+Shldr S-Frame 3.2mm Variable Perf w/ Integrated Shim FDA UDI

Identifiers

Catalog Number
RT-A892KYSDF FDA UDI
Primary DI / UDI-DI
10841962118047 EUDAMEDFDA UDI
Basic UDI-DI
8419621RTTHERMOPF EUDAMED
FDA Product Code
IYE FDA UDI
EMDN Code
Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
GMDN Term
Patient positioning thermoplastic mould material FDA UDI

Classification

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

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Depth — 3.2 Millimeter FDA UDI

Category: Patient positioning thermoplastic mould material

Fibreplast® Variable Perf™ Assure™ Open View with Integrated Shim™ by Qfix — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Patient positioning thermoplastic mould material.

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 07c51f2a-184b-477d-aa1e-81f3b7605a5d 36 fields · synced Jul 20, 2026
  • EUDAMED b81e33dc-bd29-4535-be65-7b1212f857bc 61 fields · synced Jul 20, 2026