Techno-Aide

FDA UDI

Class I (US FDA UDI)

by Techno-Aide, Inc.

Identity

Trade Name: Techno-Aide FDA UDI
Generic Name: Freestanding patient positioner, reusable FDA UDI
Device Name: SANDSOCK: 6 X 20, 10LBS FDA UDI
Model / Reference: SS-10R FDA UDI
Description: SANDSOCK: 6 X 20, 10LBS FDA UDI

Identifiers

Catalog Number: SS-10R FDA UDI
Primary DI / UDI-DI: G242SS10R9 FDA UDI
FDA Product Code: CCX FDA UDI
GMDN Term: Freestanding patient positioner, 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: Freestanding patient positioner, reusable

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

Similar devices

Also classified as Freestanding patient positioner, reusable.

Inspired by Drive — Drive Devilbiss Healthcare · Class I
Coulmed — COULMED PRODUCTS GROUP LLC · Class I
Rayshield — AADCO MEDICAL, INC. · Class I
Action® — Action Products, Inc. · Class I
Rayshield — AADCO MEDICAL, INC. · Class I
PILLING — TELEFLEX INCORPORATED · Class II
Rayshield — AADCO MEDICAL, INC. · Class I
Coulmed — COULMED PRODUCTS GROUP LLC · 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

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

Manufacturer

Manufacturer: Techno-Aide, Inc.

Sources (1)

FDA UDI 3436d6ff-72bd-4937-92c6-612f9290e261 35 fields · synced Jun 8, 2026