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FaceLake

FDA UDI

Class II (US FDA UDI)

by Lorte Technologies, Inc

Identity

Trade Name
FaceLake FDA UDI
Generic Name
Foetal Doppler system FDA UDI
Device Name
JPD-100B Ultrasonic Doppler Fetal Heartbeat Detector is an equipment to detect the fetal heartbeat in the body of the pregnant woman. FDA UDI
Model / Reference
FL-100B FDA UDI
Description
JPD-100B Ultrasonic Doppler Fetal Heartbeat Detector is an equipment to detect the fetal heartbeat in the body of the pregnant woman. FDA UDI

Identifiers

Primary DI / UDI-DI
00851908007093 FDA UDI
510(k) Number
K131457 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Foetal Doppler system

FaceLake by Lorte Technologies, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal Doppler system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 159eff7e-797b-4f3f-a580-573d5c03b70e 35 fields · synced May 30, 2026