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Magnum

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
MAGNUM FDA UDI
Generic Name
Side-notch biopsy gun needle FDA UDI
Device Name
MAGNUM® Disposable Core Tissue Biopsy Needle, 12g x 20cm FDA UDI
Model / Reference
MN1220 FDA UDI
Description
MAGNUM® Disposable Core Tissue Biopsy Needle, 12g x 20cm FDA UDI

Identifiers

Catalog Number
MN1220 FDA UDI
Primary DI / UDI-DI
00801741084232 FDA UDI
FDA Product Code
FCG FDA UDI
GMDN Term
Side-notch biopsy gun needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 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
Length — 20 Centimeter FDA UDI
Needle Gauge — 12 Gauge FDA UDI

Category: Side-notch biopsy gun needle

Magnum by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Side-notch biopsy gun needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Peripheral Vascular

Sources (1)

  • FDA UDI cc1c18c5-56a4-4716-a3fc-64242a255d93 36 fields · synced Jun 6, 2026