← Back to catalogue

Techno-Aide

FDA UDI

Class I (US FDA UDI)

by Techno-Aide, Inc.

Identity

Trade Name
Techno-Aide FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
DISPOSABLE TOP FOLD X-RAY PANEL/ FDA UDI
Model / Reference
CCM-10 FDA UDI
Description
DISPOSABLE TOP FOLD X-RAY PANEL/ FDA UDI

Identifiers

Catalog Number
CCM-10 FDA UDI
Primary DI / UDI-DI
G242CCM109 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

FDA UDI

Category: Medical equipment/instrument drape, single-use

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

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

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
Techno-Aide, Inc.

Sources (1)

  • FDA UDI 6f04dc13-9328-49eb-8bf2-844b98ccfb58 35 fields · synced Jun 1, 2026