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Provox Adhesive OptiDerm Plus

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 7332

by Atos Medical Inc.

Identity

Trade Name
Provox Adhesive OptiDerm Plus EUDAMEDFDA UDI
Generic Name
Removable ambulatory appliance skin-adherent patch FDA UDI
Device Name
Provox Adhesive EUDAMED
The Provox Adhesives are single use devices intended for laryngectomized patients breathing through a tracheostoma. The devices are attached to the skin around the tracheostoma in order to provide attachment for components of the Provox HME System. FDA UDI
Model / Reference
7332 EUDAMEDFDA UDI
Description
The Provox Adhesives are single use devices intended for laryngectomized patients breathing through a tracheostoma. The devices are attached to the skin around the tracheostoma in order to provide attachment for components of the Provox HME System. FDA UDI

Identifiers

Catalog Number
7332 FDA UDI
Primary DI / UDI-DI
07331791008177 EUDAMEDFDA UDI
Basic UDI-DI
7331791-ADH-0-000-0000-CQ EUDAMED
Unit of Use DI
07331791016912 EUDAMED
FDA Product Code
KGX FDA UDI
EMDN Code
R060280 HUMIDIFICATION SYSTEMS - ACCESSORIES EUDAMED
GMDN Term
Removable ambulatory appliance skin-adherent patch FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5240 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Removable ambulatory appliance skin-adherent patch

Provox Adhesive OptiDerm Plus by Atos Medical Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Removable ambulatory appliance skin-adherent patch.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atos Medical Inc.

Sources (2)

  • FDA UDI dd01c6fd-2785-4377-b843-c2dc21fc3ccc 36 fields · synced Aug 3, 2026
  • EUDAMED 967f63a3-5f31-4f32-a271-72386c459a15 61 fields · synced Aug 3, 2026