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Cetro America Toco Transducer for HP8040

FDA UDI

Class II (US FDA UDI)

by Cetro America

Identity

Trade Name
Cetro America Toco Transducer for HP8040 FDA UDI
Generic Name
Tocodynamometer probe FDA UDI
Device Name
Replacement Toco Transducer for HP/Philips model HP8040 fetal monitors. FDA UDI
Model / Reference
8032025 FDA UDI
Description
Replacement Toco Transducer for HP/Philips model HP8040 fetal monitors. FDA UDI

Identifiers

Primary DI / UDI-DI
00852519007359 FDA UDI
510(k) Number
K050826 FDA UDI
FDA Product Code
HGM FDA UDI
GMDN Term
Tocodynamometer probe 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tocodynamometer probe

Cetro America Toco Transducer for HP8040 by Cetro America — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tocodynamometer probe.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cetro America

Sources (1)

  • FDA UDI 5e0676d9-746c-45fb-9e5d-7c7bca1de934 35 fields · synced Jun 8, 2026