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Access™ Clearvue™

FDA UDI

Class II (US FDA UDI)

by Qfix

Identity

Trade Name
Access™ Clearvue™ FDA UDI
Generic Name
Radiological breast positioner, non-wearable FDA UDI
Device Name
Access ClearVue Prone Breast Device (17.5 cm height) FDA UDI
Model / Reference
RT-4545CV-17 FDA UDI
Description
Access ClearVue Prone Breast Device (17.5 cm height) FDA UDI

Identifiers

Catalog Number
RT-4545CV-17 FDA UDI
Primary DI / UDI-DI
10841962110607 FDA UDI
FDA Product Code
IYE FDA UDI
GMDN Term
Radiological breast positioner, non-wearable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Dimensions & Sizes

Size
Height — 17.5 Centimeter FDA UDI

Category: Radiological breast positioner, non-wearable

Access™ Clearvue™ by Qfix — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological breast positioner, non-wearable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Qfix

Sources (1)

  • FDA UDI dfb2bb8e-1c24-4547-af64-b4e1e59ef8f4 36 fields · synced May 30, 2026