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Summit

FDA UDI

Class I (US FDA UDI)

by Summit Industries, Llc

Identity

Trade Name
Summit FDA UDI
Generic Name
X-ray system tube support, floor standing FDA UDI
Device Name
RADIOGRAPHIC TUBESTAND FDA UDI
Model / Reference
S105 FDA UDI
Description
RADIOGRAPHIC TUBESTAND FDA UDI

Identifiers

Catalog Number
S105 FDA UDI
Primary DI / UDI-DI
B307S1050 FDA UDI
FDA Product Code
IYB FDA UDI
GMDN Term
X-ray system tube support, floor standing 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

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: X-ray system tube support, floor standing

Summit by Summit Industries, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray system tube support, floor standing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f330f56-51b5-4304-9aac-ab525d76612b 36 fields · synced May 30, 2026