Techno-Aide

FDA UDI

Class I (US FDA UDI)

by Techno-Aide, Inc.

Identity

Trade Name: Techno-Aide FDA UDI
Generic Name: X-ray film cassette holder FDA UDI
Device Name: MOBILE CASS/CR HOLDER:EXT-ARM (SPR) FDA UDI
Model / Reference: MCH-37C FDA UDI
Description: MOBILE CASS/CR HOLDER:EXT-ARM (SPR) FDA UDI

Identifiers

Catalog Number: MCH-37C FDA UDI
Primary DI / UDI-DI: G242MCH37C9 FDA UDI
FDA Product Code: EGZ FDA UDI
GMDN Term: X-ray film cassette holder FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.1905 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: X-ray film cassette holder

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

Similar devices

Also classified as X-ray film cassette holder.

QT-LCH — CARESTREAM HEALTH, INC. · Class I
SEDECAL — Sedecal., Sa. · Class I
Mindray — Nanjing Mindray Bio-Medical Electronics Co., Ltd · Class I
dose-map™ — Ashland Specialty Ingredients, G.P. · Class II
Q-DRT-DRXT-R — CARESTREAM HEALTH, INC. · Class II
OPERON — STRYKER Communications, Inc. · Class I
LLD 129 Compact — Drtech Corp. · Class I
dose-map™ — Ashland Specialty Ingredients, G.P. · Class II

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 d28f73bd-5bac-4248-a1b6-e326f3125f07 35 fields · synced Jun 7, 2026