← Back to catalogue

Biopsy Bracket

FDA UDI

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
Biopsy Bracket FDA UDI
Generic Name
Ultrasound imaging system tracking positioner, reusable FDA UDI
Device Name
Reusable non-sterile Verza™ bracket for use with Esaote L 8-24 transducers FDA UDI
Model / Reference
639-072 FDA UDI
Description
Reusable non-sterile Verza™ bracket for use with Esaote L 8-24 transducers FDA UDI

Identifiers

Catalog Number
639-072 FDA UDI
Primary DI / UDI-DI
00841436125055 FDA UDI
510(k) Number
K160806 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Ultrasound imaging system tracking positioner, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultrasound imaging system tracking positioner, reusable

Biopsy Bracket 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

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

Manufacturer

Sources (1)

  • FDA UDI 140ff1a4-cd05-44ad-a6a5-783f1c31f683 37 fields · synced Jun 8, 2026