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True Speed Bucky

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
True Speed Bucky FDA UDI
Generic Name
Moving x-ray grid FDA UDI
Device Name
R30-17B BUCKY: 17 X 17 RECIPROCATING FDA UDI
Model / Reference
True Speed Bucky FDA UDI
Description
R30-17B BUCKY: 17 X 17 RECIPROCATING FDA UDI

Identifiers

Catalog Number
6573737 FDA UDI
Primary DI / UDI-DI
60889976573730 FDA UDI
FDA Product Code
IXJ FDA UDI
GMDN Term
Moving x-ray grid FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1910 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

No

FDA UDI

Category: Moving x-ray grid

True Speed Bucky by Carestream Health, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Moving x-ray grid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fcc8d630-e233-4e76-83e6-b727b6fbaded 34 fields · synced Jun 8, 2026