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Kangaroo

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kangaroo FDA UDI
Generic Name
Frame/rail/pole device holder FDA UDI
Device Name
CONNECT POLE CLAMP FDA UDI
Model / Reference
384492 FDA UDI
Description
CONNECT POLE CLAMP FDA UDI

Identifiers

Catalog Number
384492 FDA UDI
Primary DI / UDI-DI
10192253007282 FDA UDI
FDA Product Code
LZH FDA UDI
GMDN Term
Frame/rail/pole device holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5725 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: Frame/rail/pole device holder

Kangaroo by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Frame/rail/pole device holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e9097290-5680-4939-81c4-3c2563171293 35 fields · synced Jun 6, 2026