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ProSomnus

EUDAMEDFDA UDI

Class I (EU MDR)

Ref [IA] with PM

by ProSomnus Sleep Technologies

Identity

Trade Name
ProSomnus EUDAMED
Prosomnus IA with Patient Monitoring FDA UDI
Generic Name
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI
Device Name
Basic obstructive sleep apnea devices with patient monitoring EUDAMED
Obstructive Sleep Apnea with Iterative Adjustment and Patient Monitoring FDA UDI
Model / Reference
[IA] with PM EUDAMED
IA Monogram Monitor FDA UDI
Description
Obstructive Sleep Apnea with Iterative Adjustment and Patient Monitoring FDA UDI

Identifiers

Primary DI / UDI-DI
00863039000430 EUDAMEDFDA UDI
Basic UDI-DI
08630390004OSAPMSM EUDAMED
510(k) Number
K161624 FDA UDI
FDA Product Code
PLC FDA UDI
EMDN Code
Q03010299 ANTISNORING AND OBSTRUCTIVE SLEEP APNOEA DEVICES - OTHER EUDAMED
GMDN Term
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.5570 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

ProSomnus by ProSomnus Sleep Technologies — 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
US-MF-000034424
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 3e1f614f-fcc9-423e-a8d1-62c6fd6a93a9 61 fields · synced Oct 6, 2026
  • FDA UDI 10c906f3-85ac-443f-b0f1-8f7f8516444c 34 fields · synced May 30, 2026