← Back to catalogue

ARES 620 Respiration Effort System

FDA UDI

Class II (US FDA UDI)

by WATERMARK MEDICAL Inc

Identity

Trade Name
ARES 620 Respiration Effort System FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
ARES 620 Resp Effort System Kit FDA UDI
Model / Reference
620 FDA UDI
Description
ARES 620 Resp Effort System Kit FDA UDI

Identifiers

Catalog Number
W17327 FDA UDI
Primary DI / UDI-DI
00854485007173 FDA UDI
510(k) Number
K160499 FDA UDI
FDA Product Code
MNR FDA UDI
GMDN Term
Home-use sleep apnoea recording system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Commercial Distribution
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

Yes

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

Category: Home-use sleep apnoea recording system

ARES 620 Respiration Effort System by WATERMARK MEDICAL Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use sleep apnoea recording system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI 6a75e90d-dd80-4fa6-ba97-449a1918170e 37 fields · synced Jun 1, 2026