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0.7/1.3u163c-36

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref 582-24780-62

by Shimadzu Corporation

Identity

Trade Name
0.7/1.3U163C-36 EUDAMEDFDA UDI
Generic Name
X-ray tube housing assembly, diagnostic FDA UDI
Device Name
X-ray tube assembly 0.7/1.3U163C-36 EUDAMED
Model / Reference
582-24780-62 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04540217059478 EUDAMEDFDA UDI
Basic UDI-DI
B-04540217059478 EUDAMED
FDA Product Code
ITY FDA UDI
EMDN Code
Z11039012 X-RAY TUBE ASSEMBLY EUDAMED
GMDN Term
X-ray tube housing assembly, diagnostic FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class I FDA UDI
Regulation Number
892.1760 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

0.7/1.3u163c-36 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 1b974539-ecf6-4bc2-8810-c8632540777a 61 fields · synced Jun 18, 2026
  • FDA UDI 8f8d5fa6-421d-445c-a968-fd623924a505 32 fields · synced May 30, 2026