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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
Limb/torso/head restraint, reusable FDA UDI
Device Name
Body Restraint Strap, Rail Mtd ULTRA-ORCHARD FDA UDI
Model / Reference
7001084-00-224 FDA UDI
Description
Body Restraint Strap, Rail Mtd ULTRA-ORCHARD FDA UDI

Identifiers

Catalog Number
7001084-00-224 FDA UDI
Primary DI / UDI-DI
10840118403914 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Limb/torso/head restraint, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Limb/torso/head restraint, reusable

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

Similar devices

Also classified as Limb/torso/head restraint, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aebb3c8a-6067-432d-9472-d1580b3d3a4b 35 fields · synced May 30, 2026