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Magic3™ Intermittent Catheter

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Magic3™ Intermittent Catheter FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
Magic3™ Intermittent Catheter Antibacterial Hydrophilic Coated Silicone, Female FDA UDI
Model / Reference
51520 FDA UDI
Description
Magic3™ Intermittent Catheter Antibacterial Hydrophilic Coated Silicone, Female FDA UDI

Identifiers

Catalog Number
51520 FDA UDI
Primary DI / UDI-DI
00801741068218 FDA UDI
FDA Product Code
MJC FDA UDI
GMDN Term
Single-administration urethral drainage 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

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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 — 20 French FDA UDI

Category: Single-administration urethral drainage catheter

Magic3™ Intermittent Catheter by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Single-administration urethral 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 938f63cc-fe2f-4733-b0b4-75c01afed7eb 36 fields · synced May 31, 2026