Techno-Aide

FDA UDI

Class I (US FDA UDI)

by Techno-Aide, Inc.

Identity

Trade Name: Techno-Aide FDA UDI
Generic Name: Limb/torso/head restraint, reusable FDA UDI
Device Name: RADIOLUCENT IMMOBILIZER STRAP 96 INCH FDA UDI
Model / Reference: RIS-96 FDA UDI
Description: RADIOLUCENT IMMOBILIZER STRAP 96 INCH FDA UDI

Identifiers

Catalog Number: RIS-96 FDA UDI
Primary DI / UDI-DI: G242RIS969 FDA UDI
FDA Product Code: CCX FDA UDI
GMDN Term: Limb/torso/head restraint, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.6820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Limb/torso/head restraint, reusable

Techno-Aide by Techno-Aide, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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POSEY — POSEY PRODUCTS, LLC · Class I
Morrison Medical — MORRISON MEDICAL, LTD · Class I
Restraint strap — Skytron, LLC · Class I
E.M Adams co, inc. — E.M. Adams · Class I
MORRISON MEDICAL — MORRISON MEDICAL, LTD · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Techno-Aide, Inc.

Sources (1)

FDA UDI 18dbb737-6590-492f-8211-884fe85ccb3c 35 fields · synced Jun 1, 2026