← Back to catalogue

Summit Radiographic Mobile Table

FDA UDI

Class II (US FDA UDI)

by Summit Industries, Llc

Identity

Trade Name
Summit Radiographic Mobile Table FDA UDI
Generic Name
Basic diagnostic x-ray system table, non-powered FDA UDI
Device Name
Table Radiologic, stationary top (892.1980) FDA UDI
Model / Reference
ST1000 FDA UDI
Description
Table Radiologic, stationary top (892.1980) FDA UDI

Identifiers

Catalog Number
ST1000 FDA UDI
Primary DI / UDI-DI
B307ST10000 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Basic diagnostic x-ray system table, non-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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: Basic diagnostic x-ray system table, non-powered

Summit Radiographic Mobile Table by Summit Industries, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic diagnostic x-ray system table, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI d0ad23e4-6993-4e89-8a16-c78237d304c2 36 fields · synced Jun 8, 2026