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Biopsy Brackt

FDA UDI

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
Biopsy Brackt FDA UDI
Generic Name
Ultrasound imaging system tracking positioner, reusable FDA UDI
Device Name
Reusable non-sterile single-angle bracket for use with Philips Ergo C5-2 transducers FDA UDI
Model / Reference
667-179 FDA UDI
Description
Reusable non-sterile single-angle bracket for use with Philips Ergo C5-2 transducers FDA UDI

Identifiers

Catalog Number
667-179 FDA UDI
Primary DI / UDI-DI
00841436120197 FDA UDI
510(k) Number
K093713 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Ultrasound imaging system tracking positioner, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultrasound imaging system tracking positioner, reusable

Biopsy Brackt by Civco Medical Instruments Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasound imaging system tracking positioner, reusable.

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 914b179a-67d2-4d3c-b93a-95088f24e0e5 37 fields · synced Jun 8, 2026