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Summit Radiographic table

FDA UDI

Class II (US FDA UDI)

by Summit Industries, Llc

Identity

Trade Name
Summit Radiographic table FDA UDI
Generic Name
Basic diagnostic x-ray system table, powered FDA UDI
Device Name
Table, Powered (892.1980) FDA UDI
Model / Reference
S211 FDA UDI
Description
Table, Powered (892.1980) FDA UDI

Identifiers

Catalog Number
S211 FDA UDI
Primary DI / UDI-DI
B307S2110 FDA UDI
FDA Product Code
IZZ FDA UDI
GMDN Term
Basic diagnostic x-ray system table, 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, powered

Summit Radiographic 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, powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ee9a96ad-3e22-4ce0-883d-9d073566d622 36 fields · synced Jun 1, 2026