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Mti

FDA UDI

Class I (US FDA UDI)

by Medical Technology Industries, Inc.

Identity

Trade Name
MTI FDA UDI
Generic Name
Operating room stool FDA UDI
Device Name
Stool, Hydraulic Pump w/o Backrest, ULTRA-SCHOONER FDA UDI
Model / Reference
328-00-226 FDA UDI
Description
Stool, Hydraulic Pump w/o Backrest, ULTRA-SCHOONER FDA UDI

Identifiers

Catalog Number
328-00-226 FDA UDI
Primary DI / UDI-DI
10840118423936 FDA UDI
FDA Product Code
FZM FDA UDI
GMDN Term
Operating room stool FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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: Operating room stool

Mti by Medical Technology Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room stool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI dde5e9be-5c84-44ad-9afb-660f7165d91f 35 fields · synced May 30, 2026