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SenoMark® Ultra Breast Tissue Marker

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
SenoMark® Ultra Breast Tissue Marker FDA UDI
Generic Name
Radiological image marker, implantable FDA UDI
Device Name
SENOMARK® ULTRA Breast Tissue Marker, 10 Ga EnCor, BioDur Coil FDA UDI
Model / Reference
SMEC10C FDA UDI
Description
SENOMARK® ULTRA Breast Tissue Marker, 10 Ga EnCor, BioDur Coil FDA UDI

Identifiers

Catalog Number
SMEC10C FDA UDI
Primary DI / UDI-DI
00801741032028 FDA UDI
510(k) Number
K123911 FDA UDI
FDA Product Code
NEU FDA UDI
GMDN Term
Radiological image marker, implantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4300 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 10 Gauge FDA UDI

Category: Radiological image marker, implantable

SenoMark® Ultra Breast Tissue Marker by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological image marker, implantable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20bc2d69-5a4f-432b-8b1b-f12fcf1fa054 38 fields · synced May 31, 2026