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TruAdvance

FDA UDI

Class II (US FDA UDI)

by H R Pharmaceuticals, Inc.

Identity

Trade Name
TruAdvance FDA UDI
Generic Name
Urethral catheterization support kit, urinary drainage FDA UDI
Device Name
TruAdvance™ Closed System Intermittent Catheter Tray FDA UDI
Model / Reference
TAS14 FDA UDI
Description
TruAdvance™ Closed System Intermittent Catheter Tray FDA UDI

Identifiers

Primary DI / UDI-DI
00850058254760 FDA UDI
FDA Product Code
OHR FDA UDI
GMDN Term
Urethral catheterization support kit, urinary drainage 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urethral catheterization support kit, urinary drainage

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

Similar devices

Also classified as Urethral catheterization support kit, urinary drainage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 70645912-0440-468b-9943-b7513d360818 34 fields · synced May 30, 2026