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TOCO Transducer

FDA UDI

Class II (US FDA UDI)

by Edan Instruments, Inc.

Identity

Trade Name
TOCO Transducer FDA UDI
Generic Name
Tocodynamometer probe FDA UDI
Model / Reference
Blue label FDA UDI

Identifiers

Primary DI / UDI-DI
06944413805507 FDA UDI
FDA Product Code
HGL FDA UDI
GMDN Term
Tocodynamometer probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2960 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tocodynamometer probe

TOCO Transducer by Edan Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tocodynamometer probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1cda0cf8-fe90-4be3-8090-b6979678ef47 32 fields · synced May 30, 2026