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Ritter

FDA UDI

Class I (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Ritter FDA UDI
Generic Name
Examination/treatment table, manual FDA UDI
Device Name
The 203 Treatment Table is constructed of steel from its frame to its legs, and its flat top is designed to provide a stable, solid surface for patient manipulations or adjustments during examinations. FDA UDI
Model / Reference
203-011 FDA UDI
Description
The 203 Treatment Table is constructed of steel from its frame to its legs, and its flat top is designed to provide a stable, solid surface for patient manipulations or adjustments during examinations. FDA UDI

Identifiers

Catalog Number
203-011 FDA UDI
Primary DI / UDI-DI
00841709109027 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Examination/treatment table, manual

Ritter by Midmark Corporation — 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

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 856450ed-5dac-40b9-9639-cf63c0462817 35 fields · synced Jun 8, 2026