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Ch-200

FDA UDI

Class I (US FDA UDI)

by Shimadzu Corp.

Identity

Trade Name
CH-200 FDA UDI
Generic Name
X-ray system tube support, ceiling mounted FDA UDI
Model / Reference
503-58100-27 FDA UDI

Identifiers

Primary DI / UDI-DI
04540217014491 FDA UDI
FDA Product Code
IYB FDA UDI
GMDN Term
X-ray system tube support, ceiling mounted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1770 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

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

Category: X-ray system tube support, ceiling mounted

Ch-200 by Shimadzu Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray system tube support, ceiling mounted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shimadzu Corp.

Sources (1)

  • FDA UDI c76bb3dd-3f31-4192-b972-26142f5c6702 32 fields · synced Jun 1, 2026