← Back to catalogue

System One Heated Tube Humidfier IT

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref IT6TModel System One Heated Humidifier

by Respironics Inc.

Identity

Trade Name
System One Heated Tube Humidfier IT EUDAMED
System One Humidifier FDA UDI
Generic Name
Heated respiratory humidifier FDA UDI
Device Name
System One Heated Tube Humidifier, Italy FDA UDI
Model / Reference
System One Heated Humidifier EUDAMED
IT6T EUDAMED
System One Heated Tube Humidifier, IT FDA UDI
Description
System One Heated Tube Humidifier, Italy FDA UDI

Identifiers

Catalog Number
IT6T FDA UDI
Primary DI / UDI-DI
00606959048249 EUDAMEDFDA UDI
Basic UDI-DI
B-00606959048249 EUDAMED
510(k) Number
K113068 FDA UDI
FDA Product Code
BZD FDA UDI
EMDN Code
R060201 ACTIVE VENTILATION HUMIDIFICATION SYSTEMS, EUDAMED
GMDN Term
Heated respiratory humidifier FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.5905 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

System One Heated Tube Humidfier IT by Respironics, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Respironics Inc.
EUDAMED SRN
US-MF-000002301
Authorised Representative
Respironics Deutschland GmbH & Co.KG DE-AR-000006164

Sources (3)

  • EUDAMED 4334078e-2227-446d-b66d-133249795ec8 61 fields · synced Jun 18, 2026
  • FDA UDI 0707d046-6176-4c20-b72c-c72e85ac829e 37 fields · synced May 30, 2026
  • EUDAMED ead516c0-4248-428d-9a7e-db5b90c42e4d 61 fields · synced Jun 18, 2026