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Aquarius CTS

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref AQS2002

by Laborie Medical Technologies Canada ULC

Identity

Trade Name
Aquarius Urodynamic Analyzer System EUDAMED
Aquarius CTS FDA UDI
Generic Name
Urodynamic measurement system FDA UDI
Device Name
Aquarius Urodynamics Analyzer System EUDAMED
Model / Reference
AQS2002 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00627825003704 EUDAMEDFDA UDI
Basic UDI-DI
B-00627825003704 EUDAMED
FDA Product Code
FEN FDA UDI
EMDN Code
Z12160401 URODYNAMICS SYSTEMS EUDAMED
GMDN Term
Urodynamic measurement system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
876.1620 FDA UDI
Market of Registration
Netherlands 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urodynamic measurement system

Aquarius CTS by Laborie Medical Technologies Canada ULC — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Urodynamic measurement system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 0e974a9a-9375-4a26-b55b-f9b5ffbd38d8 32 fields · synced Jul 8, 2026
  • EUDAMED 1687597b-187a-454c-be50-4cee7755e5a9 61 fields · synced Jul 8, 2026