← Back to catalogue

Magic3 Go Male Catheter with SureGrip

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
Magic3 Go Male Catheter with SureGrip FDA UDI
Generic Name
Single-administration urethral drainage catheter FDA UDI
Device Name
Magic3 Go 20 Fr Male Catheter with SureGrip FDA UDI
Model / Reference
53820G FDA UDI
Description
Magic3 Go 20 Fr Male Catheter with SureGrip FDA UDI

Identifiers

Catalog Number
53820G FDA UDI
Primary DI / UDI-DI
00801741136993 FDA UDI
FDA Product Code
EZD 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

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 — 20 French FDA UDI

Category: Single-administration urethral drainage catheter

Magic3 Go Male Catheter with SureGrip 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI 1fe2253b-6cf8-43db-af0c-32a363b04593 36 fields · synced Jun 1, 2026