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Sherlock 3CG+ TCS on Site~Rite Halcyon

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Sherlock 3CG+ TCS on Site~Rite Halcyon FDA UDI
Generic Name
Central venous catheter navigation system, electrocardiographic FDA UDI
Device Name
Sherlock 3CG+ Tip Confirmation System (TCS) Integrated on Site~Rite Halcyon Ultrasound System FDA UDI
Model / Reference
S3CG+ Hal v 3.0.0 FDA UDI
Description
Sherlock 3CG+ Tip Confirmation System (TCS) Integrated on Site~Rite Halcyon Ultrasound System FDA UDI

Identifiers

Catalog Number
S3CG+ Hal v 3.0.0 FDA UDI
Primary DI / UDI-DI
00801741183393 FDA UDI
FDA Product Code
LJS FDA UDI
GMDN Term
Central venous catheter navigation system, electrocardiographic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5970 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

No

FDA UDI

Category: Central venous catheter navigation system, electrocardiographic

Sherlock 3CG+ TCS on Site~Rite Halcyon 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 67602bae-24f9-4265-9059-6006dd29393e 35 fields · synced Jun 9, 2026