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Site~Rite 8 Ultrasound System

FDA UDI

Class II (US FDA UDI)

by Bard Access Systems, Inc.

Identity

Trade Name
Site~Rite 8 Ultrasound System FDA UDI
Generic Name
Medical device service rail clamp FDA UDI
Device Name
Cue Mounting Arm FDA UDI
Model / Reference
9770605 FDA UDI
Description
Cue Mounting Arm FDA UDI

Identifiers

Catalog Number
9770605 FDA UDI
Primary DI / UDI-DI
00801741138256 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Medical device service rail clamp 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

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

Yes

FDA UDI

Category: Medical device service rail clamp

Site~Rite 8 Ultrasound System by Bard Access Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device service rail clamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7861f88f-3445-4e20-8fdf-adf57186fb89 36 fields · synced Jun 9, 2026