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Element Treatment Table

FDA UDI

Class I (US FDA UDI)

by The Brewer Company LLC

Identity

Trade Name
Element Treatment Table FDA UDI
Generic Name
Examination/treatment table, manual FDA UDI
Device Name
These tables are designed to provide positioning and support of patients during general examinations conducted by qualified medical professionals. FDA UDI
Model / Reference
2010 FDA UDI
Description
These tables are designed to provide positioning and support of patients during general examinations conducted by qualified medical professionals. FDA UDI

Identifiers

Catalog Number
2010 FDA UDI
Primary DI / UDI-DI
07285640020103 FDA UDI
FDA Product Code
FRK FDA UDI
GMDN Term
Examination/treatment table, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 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

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Examination/treatment table, manual

Element Treatment Table by The Brewer Company LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Examination/treatment table, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc9f9866-23fa-4024-b577-f1af5117590b 35 fields · synced Jun 9, 2026