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Totalis™ Rigid Endo Kit

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Totalis™ Rigid Endo Kit FDA UDI
Generic Name
Ureteral patency kit FDA UDI
Device Name
Totalis™ Rigid Endo Kit with InLay® Ureteral Stent, EcoFlex™ Stone Basket and NiCore® Nitinol Guidewire FDA UDI
Model / Reference
REK26N FDA UDI
Description
Totalis™ Rigid Endo Kit with InLay® Ureteral Stent, EcoFlex™ Stone Basket and NiCore® Nitinol Guidewire FDA UDI

Identifiers

Catalog Number
REK26N FDA UDI
Primary DI / UDI-DI
00801741097584 FDA UDI
FDA Product Code
FAD FDA UDI
GMDN Term
Ureteral patency kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4620 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 26 Centimeter FDA UDI
Catheter Gauge — 6 French FDA UDI

Category: Ureteral patency kit

Totalis™ Rigid Endo Kit by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ureteral patency kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 75eb3b36-1f38-4b42-9daa-195c1d6767d8 36 fields · synced Jun 8, 2026