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YosemiteView 3643W

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 104Model CareView 1800RF

by CareRay Digital Medical Technology Co., Ltd.

Identity

Trade Name
YosemiteView 3643W EUDAMED
X-ray Flat Panel Detector FDA UDI
Generic Name
Stationary basic diagnostic x-ray system, digital FDA UDI
Device Name
X-ray Flat Panel Detector EUDAMED
Model / Reference
CareView 1800RF EUDAMED
104 EUDAMED
YosemiteView 3643W FDA UDI

Identifiers

Primary DI / UDI-DI
06970597831049 EUDAMEDFDA UDI
Basic UDI-DI
697059783DynamicCR EUDAMED
Direct Marketing DI
06970597831049 EUDAMED
510(k) Number
K232058 FDA UDI
FDA Product Code
MQB FDA UDI
JAA FDA UDI
EMDN Code
Z11031101 MULTIFUNCTIONAL SYSTEMS FOR DIRECT DIGITAL RADIOLOGY EUDAMED
GMDN Term
Stationary basic diagnostic x-ray system, digital FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
892.1680 FDA UDI
892.1650 FDA UDI
Market of Registration
Northern Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Stationary basic diagnostic x-ray system, digital

YosemiteView 3643W by Careray Digital Medical Technology Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, digital.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000007229
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED aa835968-d003-4d3b-b941-9b4b16e0d0db 61 fields · synced Aug 2, 2026
  • FDA UDI 61bf7f73-d950-4c43-9d03-06fa9dfca8b1 33 fields · synced May 30, 2026