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Koala® Cables

FDA UDI

Class II (US FDA UDI)

by Clinical Innovations, LLC

Identity

Trade Name
Koala® Cables FDA UDI
Generic Name
Intrapartum pressure monitoring catheter FDA UDI
Device Name
Cables to IUP catheters: Edan F6 FDA UDI
Model / Reference
IPC-5090 FDA UDI
Description
Cables to IUP catheters: Edan F6 FDA UDI

Identifiers

Primary DI / UDI-DI
00814247020277 FDA UDI
510(k) Number
K974389 FDA UDI
FDA Product Code
HFN FDA UDI
GMDN Term
Intrapartum pressure monitoring catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2700 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: Intrapartum pressure monitoring catheter

Koala® Cables by Clinical Innovations, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intrapartum pressure monitoring catheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 626de4e6-826d-43f0-82b5-50b66871ed54 34 fields · synced Jun 9, 2026