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Q-Snor Microphone

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 0545Model 0546

by BRAEBON Medical Corporation

Identity

Trade Name
Q-SNOR MICROPHONE EUDAMED
BRAEBON Q-Snor Microphone FDA UDI
Generic Name
Freestanding microphone FDA UDI
Device Name
Q-Snore Kit EUDAMED
Q-Snor microphone for use during sleep disorder studies as a measure of snoring for recording onto a data acquisition system. FDA UDI
Model / Reference
0546 EUDAMED
0545 EUDAMEDFDA UDI
Description
Q-Snor microphone for use during sleep disorder studies as a measure of snoring for recording onto a data acquisition system. FDA UDI

Identifiers

Catalog Number
0545 FDA UDI
Primary DI / UDI-DI
B14005450 EUDAMEDFDA UDI
Basic UDI-DI
++B140QSnorD6 EUDAMED
Direct Marketing DI
B14005450 EUDAMED
510(k) Number
K020312 FDA UDI
FDA Product Code
MNR FDA UDI
EMDN Code
Z12100580 POLYSOMNOGRAPHY INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Freestanding microphone FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Market of Registration
Germany 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

Yes

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

Yes

FDA UDI

Q-Snor Microphone by Braebon Medical Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CA-MF-000002190
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 6fde6225-0b49-4da5-9923-b1c5725d1fac 61 fields · synced Jun 19, 2026
  • FDA UDI c474eac4-dc98-4fe9-98fd-8b83cab23f04 37 fields · synced May 30, 2026