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Site-Rite

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Site-Rite FDA UDI
Generic Name
General-purpose ultrasound imaging system FDA UDI
Device Name
Software FDA UDI
Model / Reference
SR8v1.0.2 FDA UDI
Description
Software FDA UDI

Identifiers

Catalog Number
SR8v1.0.2 FDA UDI
Primary DI / UDI-DI
00801741121432 FDA UDI
FDA Product Code
IYO FDA UDI
LLZ FDA UDI
GMDN Term
General-purpose ultrasound imaging system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 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 system

Site-Rite 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3ac78dd1-639b-4ead-b71a-dbedb7ae63b3 35 fields · synced Jun 9, 2026