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Care Mill

FDA UDI

Class II (US FDA UDI)

by Simpro

Identity

Trade Name
Care Mill FDA UDI
Generic Name
Foetal Doppler system FDA UDI
Device Name
Pocket Fetal Doppler FDA UDI
Model / Reference
Baby Sound C FDA UDI
Description
Pocket Fetal Doppler FDA UDI

Identifiers

Primary DI / UDI-DI
00810025923440 FDA UDI
FDA Product Code
KNG FDA UDI
GMDN Term
Foetal Doppler system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.2660 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Foetal Doppler system

Care Mill by Simpro — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal Doppler system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Simpro

Sources (1)

  • FDA UDI 0ef69aa7-25b0-4032-9c47-5d2b782053c1 33 fields · synced May 31, 2026