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Versa Exam Table

FDA UDI

Class I (US FDA UDI)

by The Brewer Company LLC

Identity

Trade Name
Versa Exam Table FDA UDI
Generic Name
Examination/treatment table, manual FDA UDI
Device Name
Versa products will be sold into the physician office market and are intended to be used by healthcare professionals employed by physician offices, medical clinics, and IDNs. Versa products will be used to examine a wide variety of patients of various sizes and mobility. Versa will be used inside of an office/clinic and require no special environmental needs. FDA UDI
Model / Reference
1000 FDA UDI
Description
Versa products will be sold into the physician office market and are intended to be used by healthcare professionals employed by physician offices, medical clinics, and IDNs. Versa products will be used to examine a wide variety of patients of various sizes and mobility. Versa will be used inside of an office/clinic and require no special environmental needs. FDA UDI

Identifiers

Catalog Number
1000 FDA UDI
Primary DI / UDI-DI
72856400010005 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
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 94e80488-5f0d-4ea4-a477-48777dc2e67b 36 fields · synced Jun 9, 2026