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BD SiteRite 9 Ultrasound System

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
BD SiteRite 9 Ultrasound System FDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
BD SiteRite 9 Cue Linear Probe FDA UDI
Model / Reference
9770803 FDA UDI
Description
BD SiteRite 9 Cue Linear Probe FDA UDI

Identifiers

Catalog Number
9770803 FDA UDI
Primary DI / UDI-DI
00801741226274 FDA UDI
510(k) Number
K231283 FDA UDI
FDA Product Code
ITX FDA UDI
LLZ FDA UDI
IYO FDA UDI
GMDN Term
General-purpose ultrasound imaging system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.2050 FDA UDI
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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose ultrasound imaging system

BD SiteRite 9 Ultrasound System by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose ultrasound imaging system.

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 1ed531cf-d531-4278-bab2-c3280de10870 37 fields · synced Jun 9, 2026