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Sonicaid

FDA UDI

Class II (US FDA UDI)

by Huntleigh Healthcare , Ltd.

Identity

Trade Name
SONICAID FDA UDI
Generic Name
Cardiotocography telemetric monitoring system FDA UDI
Device Name
SONICAID FREEDOM WMTS FDA UDI
Model / Reference
SF1-SL FDA UDI
Description
SONICAID FREEDOM WMTS FDA UDI

Identifiers

Catalog Number
SF1-SL FDA UDI
Primary DI / UDI-DI
05051968032133 FDA UDI
510(k) Number
K132650 FDA UDI
FDA Product Code
HGM FDA UDI
GMDN Term
Cardiotocography telemetric monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2740 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiotocography telemetric monitoring system

Sonicaid by Huntleigh Healthcare , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiotocography telemetric monitoring system.

Cleared under the same submission

K132650 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Huntleigh Healthcare , Ltd.

Sources (1)

  • FDA UDI 343e0e79-ad2c-4708-9c66-602359328f35 37 fields · synced Jun 1, 2026