Avalon TOCO MP Transducer

FDA UDI

Class II (US FDA UDI)

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name: Avalon TOCO MP Transducer FDA UDI
Generic Name: Tocodynamometer probe FDA UDI
Device Name: Toco MP Transducer including Toco and maternal Pulse Measurement FDA UDI
Model / Reference: Avalon TOCO MP Transducer FDA UDI
Description: Toco MP Transducer including Toco and maternal Pulse Measurement FDA UDI

Identifiers

Catalog Number: 989803170601 FDA UDI
Primary DI / UDI-DI: 00884838021471 FDA UDI
FDA Product Code: HFM FDA UDI
GMDN Term: Tocodynamometer probe FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.2720 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Tocodynamometer probe

Avalon TOCO MP Transducer by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Tocodynamometer probe.

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Cetro America Toco Transducer for HP 1350+, Waterproof — Cetro America · Class II
FEATHERLITE AQUA — Parker Hannifin Corp. · Class II
FEATHERLITE TOCO — Parker Hannifin Corp. · Class II
FEATHERLITE TOCO PLUS — Parker Hannifin Corp. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Philips Medizin Systeme Böblingen GmbH

Sources (1)

FDA UDI a642f761-bae5-4215-bac5-f214a3b37f1b 36 fields · synced May 30, 2026