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Peditrol

EUDAMEDFDA UDI

Class I (EU MDR)

Ref URO 041

by Wismed (PTY) Ltd

Identity

Trade Name
Peditrol EUDAMEDFDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
Peditrol EUDAMED
Peditrol is a foot-operated irrigation system that is used during Ureterorenoscopy to facilitate irrigation and manipulation of the stones. The irrigation helps to maintain a clear visual field by displacing blood, stone fragments and debris. FDA UDI
Model / Reference
URO 041 EUDAMED
1 FDA UDI
Description
Peditrol is a foot-operated irrigation system that is used during Ureterorenoscopy to facilitate irrigation and manipulation of the stones. The irrigation helps to maintain a clear visual field by displacing blood, stone fragments and debris. FDA UDI

Identifiers

Primary DI / UDI-DI
06009900408316 EUDAMEDFDA UDI
Basic UDI-DI
60099004083URO04136 EUDAMED
FDA Product Code
FFY FDA UDI
EMDN Code
Z12019007 IRRIGATORS EUDAMED
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
876.1500 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

Peditrol by Wismed (PTY) Ltd — 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

Manufacturer
Wismed (PTY) Ltd
EUDAMED SRN
ZA-MF-000035555
Authorised Representative
TNMC Devices Llc HR-AR-000019582

Sources (2)

  • EUDAMED 988bcfee-2a6a-4c70-87c2-a0ef8b583bd2 61 fields · synced Aug 4, 2026
  • FDA UDI e2681b91-fdc6-40cd-825e-57600756e159 35 fields · synced May 29, 2026