← Back to catalogue

Ritter

FDA UDI

Class I (US FDA UDI)

by Midmark Corporation

Identity

Trade Name
Ritter FDA UDI
Generic Name
General examination/treatment chair, electric FDA UDI
Device Name
The Ritter Security Belt is intended to secure patients to the table during examinations and procedures. The length and location of the straps are both adjustable allowing them to be used for patients of all sizes. FDA UDI
Model / Reference
9A214002 FDA UDI
Description
The Ritter Security Belt is intended to secure patients to the table during examinations and procedures. The length and location of the straps are both adjustable allowing them to be used for patients of all sizes. FDA UDI

Identifiers

Catalog Number
9A214002 FDA UDI
Primary DI / UDI-DI
00841709111099 FDA UDI
FDA Product Code
GBB FDA UDI
GMDN Term
General examination/treatment chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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: General examination/treatment chair, electric

Ritter by Midmark Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General examination/treatment chair, electric.

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

Manufacturer
Midmark Corporation

Sources (1)

  • FDA UDI 1c4722f0-c9a9-4e71-9741-421c9f12c867 35 fields · synced Jun 8, 2026