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Provox Life Energy HME

FDA UDIEUDAMED

Class I (US FDA UDI)

by Atos Medical Inc.

Identity

Trade Name
Provox Life Energy HME FDA UDI
Generic Name
Tracheostoma protective filter FDA UDI
Device Name
Provox Life HMEs are single use heat and moisture exchangers for patients breathing through a tracheostoma. FDA UDI
Model / Reference
8312 FDA UDI
Description
Provox Life HMEs are single use heat and moisture exchangers for patients breathing through a tracheostoma. FDA UDI

Identifiers

Catalog Number
8312 FDA UDI
Primary DI / UDI-DI
07331791013744 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Tracheostoma protective filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5375 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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: Tracheostoma protective filter

Provox Life Energy HME by Atos Medical Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Tracheostoma protective filter.

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 3081b341-abca-4e5b-80f2-e2f40fa6f962 36 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 19, 2026