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Bardex® Pezzer Model Drain

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Bardex® Pezzer Model Drain FDA UDI
Generic Name
Suprapubic drainage catheter FDA UDI
Device Name
Bardex® Pezzer Model Drain 3cm Head FDA UDI
Model / Reference
065040 FDA UDI
Description
Bardex® Pezzer Model Drain 3cm Head FDA UDI

Identifiers

Catalog Number
065040 FDA UDI
Primary DI / UDI-DI
00801741030239 FDA UDI
FDA Product Code
FEW FDA UDI
GMDN Term
Suprapubic drainage catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5090 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

Dimensions & Sizes

Size
Catheter Gauge — 40 French FDA UDI

Category: Suprapubic drainage catheter

Bardex® Pezzer Model Drain by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suprapubic drainage catheter.

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 24066bcd-8d3e-4fa5-bd5d-9cf7aaf1cab0 36 fields · synced May 30, 2026