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Sherlock 3CG+, BD SiteRite 9 Ultrasound System

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Sherlock 3CG+, BD SiteRite 9 Ultrasound System FDA UDI
Generic Name
Central venous catheter navigation system, electrocardiographic/magnetic FDA UDI
Device Name
Site~Rite 9 Ultrasound Software v.1.2.0 FDA UDI
Model / Reference
SR9v1.2.0 FDA UDI
Description
Site~Rite 9 Ultrasound Software v.1.2.0 FDA UDI

Identifiers

Catalog Number
SR9v1.2.0 FDA UDI
Primary DI / UDI-DI
00801741231186 FDA UDI
FDA Product Code
IYO FDA UDI
ITX FDA UDI
LJS FDA UDI
LLZ FDA UDI
GMDN Term
Central venous catheter navigation system, electrocardiographic/magnetic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
892.1570 FDA UDI
880.5970 FDA UDI
892.2050 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose ultrasound imaging systemCentral venous catheter navigation system, electrocardiographic/magnetic

Sherlock 3CG+, 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 Central venous catheter navigation system, electrocardiographic/magnetic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bard Access Systems, Inc.

Sources (1)

  • FDA UDI 89977dad-8844-4588-ba1d-ff094d364666 35 fields · synced Jun 9, 2026