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TruCath

FDA UDI

Class II (US FDA UDI)

by H R Pharmaceuticals, Inc.

Identity

Trade Name
TruCath FDA UDI
Generic Name
Ureteral catheter FDA UDI
Device Name
TruCath® Red Rubber Intermittent Urethral Catheter, 12 Fr, 16" Length FDA UDI
Model / Reference
RR12 FDA UDI
Description
TruCath® Red Rubber Intermittent Urethral Catheter, 12 Fr, 16" Length FDA UDI

Identifiers

Primary DI / UDI-DI
00850045818333 FDA UDI
FDA Product Code
EYB FDA UDI
GMDN Term
Ureteral catheter 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

Yes

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: Ureteral catheter

TruCath by H R Pharmaceuticals, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ureteral catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 422c30dc-fbb8-4375-8f3e-ebdeaa017997 35 fields · synced Jun 7, 2026