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Provox XtraBase Adhesive

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 7265

by Atos Medical Inc.

Identity

Trade Name
Provox XtraBase Adhesive 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. The FlexiDerm adhesives are Provox FlexiDerm Round/Oval/Plus and Provox XtraBase with a concave shaped base. FDA UDI
Model / Reference
7265 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. The FlexiDerm adhesives are Provox FlexiDerm Round/Oval/Plus and Provox XtraBase with a concave shaped base. FDA UDI

Identifiers

Catalog Number
7265 FDA UDI
Primary DI / UDI-DI
07331791001703 EUDAMEDFDA UDI
Basic UDI-DI
7331791-ADH-0-000-0000-CQ EUDAMED
Unit of Use DI
07331791016929 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
Austria 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 XtraBase Adhesive 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 04a53c90-2b89-4e5f-a175-489f3f7a68d3 36 fields · synced Jul 8, 2026
  • EUDAMED 99bb2f1c-7b7b-4cad-98a8-0e1b17fe9d98 61 fields · synced Jun 18, 2026