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RADspeed Pro

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 566-26000-21

by Shimadzu Corporation

Identity

Trade Name
RADspeed Pro EUDAMEDFDA UDI
Generic Name
Stationary basic diagnostic x-ray system, digital FDA UDI
Device Name
Digital Radiography System RADspeed Pro EUDAMED
Model / Reference
566-26000-21 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04540217064298 EUDAMEDFDA UDI
Basic UDI-DI
B-04540217064298 EUDAMED
510(k) Number
K152244 FDA UDI
FDA Product Code
KPR FDA UDI
EMDN Code
Z11030506 TELERADIOGRAPHS EUDAMED
GMDN Term
Stationary basic diagnostic x-ray system, digital FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
892.1680 FDA UDI
Market of Registration
Germany 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

RADspeed Pro by Shimadzu Corporation — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
JP-MF-000025145
Authorised Representative
Shimadzu Europa GmbH DE-AR-000013563

Sources (2)

  • EUDAMED afdbf8a1-878e-486a-b618-bcf57f6e89f5 61 fields · synced Jul 15, 2026
  • FDA UDI 6e140b3b-96a0-4c81-9aaa-59c61d2f4c70 33 fields · synced May 29, 2026