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Ghiatas®

FDA UDI

Class I (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
GHIATAS® FDA UDI
Generic Name
Radiological image marker, implantable FDA UDI
Device Name
GHIATAS® Beaded Breast Localization Wire, 20g x 5cm needle FDA UDI
Model / Reference
47520 FDA UDI
Description
GHIATAS® Beaded Breast Localization Wire, 20g x 5cm needle FDA UDI

Identifiers

Catalog Number
47520 FDA UDI
Primary DI / UDI-DI
00801741079801 FDA UDI
FDA Product Code
GDF FDA UDI
GMDN Term
Radiological image marker, implantable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Dimensions & Sizes

Size
Needle Gauge — 20 Gauge FDA UDI

Category: Radiological image marker, implantable

Ghiatas® by Bard Peripheral Vascular — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological image marker, implantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e881d6ec-dd07-4185-8ae0-62925f56e92c 36 fields · synced Jun 1, 2026