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DreamStation

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
DreamStation FDA UDI
Generic Name
Heated respiratory humidifier FDA UDI
Device Name
15 mm Heated Tube, China FDA UDI
Model / Reference
15MM Heated Tube, China FDA UDI
Description
15 mm Heated Tube, China FDA UDI

Identifiers

Catalog Number
CNHT15 FDA UDI
Primary DI / UDI-DI
00606959049826 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Heated respiratory humidifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

DreamStation by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 6098698f-3163-4b6b-acfd-d9576ea7c31a 37 fields · synced May 30, 2026