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Med-Rx

FDA UDI

Class II (US FDA UDI)

by Canadian Hospital Specialties Limited

Identity

Trade Name
MED-RX FDA UDI
Generic Name
Urological irrigation set FDA UDI
Device Name
MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET FDA UDI
Model / Reference
10-3001 FDA UDI
Description
MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET FDA UDI

Identifiers

Catalog Number
10-3001 FDA UDI
Primary DI / UDI-DI
00628725001012 FDA UDI
FDA Product Code
LJH FDA UDI
GMDN Term
Urological irrigation set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urological irrigation set

Med-Rx by Canadian Hospital Specialties Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urological irrigation set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6015e6a2-237c-4b61-91ff-185330c98554 35 fields · synced May 30, 2026