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Unimed

FDA UDI

Class II (US FDA UDI)

by Unimed Medical Supplies, Inc.

Identity

Trade Name
Unimed FDA UDI
Generic Name
Foetal Doppler system probe FDA UDI
Device Name
Philips 15245A/ 029/2.5m /INTEGRAL PROCESS FDA UDI
Model / Reference
UFU200-10 FDA UDI
Description
Philips 15245A/ 029/2.5m /INTEGRAL PROCESS FDA UDI

Identifiers

Primary DI / UDI-DI
06945664863551 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Foetal Doppler system probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 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

Yes

FDA UDI

Category: Foetal Doppler system probe

Unimed by Unimed Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal Doppler system probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d028b3b-b04c-4b7a-bb2a-c5f04fd9800a 33 fields · synced May 31, 2026