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Dual Action Pump (Foot Variant)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref URO 057

by Calyx Medical Sp. z o.o.

Identity

Trade Name
Dual Action Pump (Foot Variant) EUDAMED
Dual Action Pump Foot FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Dual Action Pump (Foot Variant) EUDAMED
The Dual Action Pump (DAP) is a user-controlled manual pump that delivers a bolus of irrigation fluid to the upper urinary tract during stone management, while simultaneously draining the same volume. FDA UDI
Model / Reference
URO 057 EUDAMED
1 FDA UDI
Description
The Dual Action Pump (DAP) is a user-controlled manual pump that delivers a bolus of irrigation fluid to the upper urinary tract during stone management, while simultaneously draining the same volume. FDA UDI

Identifiers

Primary DI / UDI-DI
05906168942211 EUDAMEDFDA UDI
Basic UDI-DI
59061689422URO057LE EUDAMED
FDA Product Code
FFD FDA UDI
EMDN Code
Z12019007 IRRIGATORS EUDAMED
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
876.4370 FDA UDI
Market of Registration
Poland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic spray catheter, single-use

Dual Action Pump (Foot Variant) by Calyx Medical Sp. z o.o. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic spray catheter, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
PL-MF-000038787

Sources (2)

  • EUDAMED f2b91a63-39f2-4b95-90aa-f61570ca5c74 61 fields · synced Jun 18, 2026
  • FDA UDI f23c2fff-a6f8-4c06-9f8f-8fb656b84eff 35 fields · synced May 30, 2026