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DreamWear Under Nose Mask Medium, Medium Frame w/o Headgear, Global

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 1116706

by Respironics Inc.

Identity

Trade Name
DreamWear Under Nose Mask Medium, Medium Frame w/o Headgear, Global EUDAMED
DreamWear FDA UDI
Generic Name
CPAP/BPAP nasal mask, reusable FDA UDI
Device Name
DreamWear Under the Nose EUDAMED
DreamWear Under the Nose Nasal Mask, Medium, with Medium Frame, without Headgear, Global FDA UDI
Model / Reference
1116706 EUDAMED
DreamWear Under Nose Mask, M, M Frame w/o Headgear, Global FDA UDI
Description
DreamWear Under the Nose Nasal Mask, Medium, with Medium Frame, without Headgear, Global FDA UDI

Identifiers

Catalog Number
1116706 FDA UDI
Primary DI / UDI-DI
00606959031036 EUDAMEDFDA UDI
Basic UDI-DI
B-00606959031036 EUDAMED
FDA Product Code
BZD FDA UDI
EMDN Code
R0301010202 NIV MASKS EUDAMED
GMDN Term
CPAP/BPAP nasal mask, reusable 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

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

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

No

FDA UDI

DreamWear Under Nose Mask Medium, Medium Frame w/o Headgear, Global by Respironics, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

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

Sources (3)

  • EUDAMED 4dd11e83-f3ce-44e5-a067-4aa29da2c57e 61 fields · synced Jun 18, 2026
  • FDA UDI 0c90a2c2-6c98-4ce6-a236-0f9795ae76b0 36 fields · synced May 27, 2026
  • EUDAMED a0b78268-d486-4880-af8c-5938430af74d 61 fields · synced Jun 18, 2026