← Back to catalogue

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/Ergo Backrest, PREMIUM-BLACK FDA UDI
Model / Reference
329-00-217 FDA UDI
Description
Stool, Hydraulic Pump w/Ergo Backrest, PREMIUM-BLACK FDA UDI

Identifiers

Catalog Number
329-00-217 FDA UDI
Primary DI / UDI-DI
10840118423127 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medical Technology Industries, Inc.

Sources (1)

  • FDA UDI 55e4d232-de70-43a6-a51a-8fd1c966daa2 35 fields · synced Jun 8, 2026