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Ameritus Transducer

FDA UDI

Class II (US FDA UDI)

by Kentec Medical, Inc.

Identity

Trade Name
Ameritus Transducer FDA UDI
Generic Name
Foetal/maternal prenatal monitor FDA UDI
Device Name
transducer FDA UDI
Model / Reference
ATG-SLIM-T FDA UDI
Description
transducer FDA UDI

Identifiers

Catalog Number
ATG-SLIM-T FDA UDI
Primary DI / UDI-DI
10817522010663 FDA UDI
510(k) Number
K043075 FDA UDI
FDA Product Code
HGM FDA UDI
GMDN Term
Foetal/maternal prenatal monitor 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: Foetal/maternal prenatal monitor

Ameritus Transducer by Kentec Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal/maternal prenatal monitor.

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 cba451c0-43d3-4992-8767-19115f41296b 36 fields · synced Jun 6, 2026