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Mothership Wireless Fetal Tocodynamometer Transducer, Button Style

FDA UDI

Class II (US FDA UDI)

by Tenacore Holdings, Inc.

Identity

Trade Name
Mothership Wireless Fetal Tocodynamometer Transducer, Button Style FDA UDI
Generic Name
Cardiotocography telemetric monitoring system transmitter FDA UDI
Device Name
Mothership Wireless Fetal Tocodynamometer Transducer, Button Style FDA UDI
Model / Reference
F1 FDA UDI
Description
Mothership Wireless Fetal Tocodynamometer Transducer, Button Style FDA UDI

Identifiers

Primary DI / UDI-DI
00852189007345 FDA UDI
FDA Product Code
HGM FDA UDI
GMDN Term
Cardiotocography telemetric monitoring system transmitter 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

Yes

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cardiotocography telemetric monitoring system transmitter

Mothership Wireless Fetal Tocodynamometer Transducer, Button Style by Tenacore Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Cardiotocography telemetric monitoring system transmitter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d88c1fb5-a3cb-4d0d-a2fa-c50a79fd7e2c 34 fields · synced Jun 6, 2026