Paryvara

FDA UDI

Class II (US FDA UDI)

by Boot Remedy Ltd

Identity

Trade Name: Paryvara FDA UDI
Generic Name: Foetal Doppler system probe FDA UDI
Device Name: Paryvara "Baby Beats" Heart Beat Monitor FDA UDI
Model / Reference: PBB-1 FDA UDI
Description: Paryvara "Baby Beats" Heart Beat Monitor FDA UDI

Identifiers

Primary DI / UDI-DI: 05060502570017 FDA UDI
FDA Product Code: KNG FDA UDI
GMDN Term: Foetal Doppler system probe 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Foetal Doppler system probe

Paryvara by Boot Remedy Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foetal Doppler system probe.

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CONTEC — Contec Medical Systems Co., Ltd. · Class II
US Transducer — Edan Instruments, Inc. · Class II
Hi-bebe — Bistos Co., Ltd. · Class II
ECO Series Diagnostic Ultrasound Systems — CHISON Medical Technologies Co., Ltd. · Class II
Phased array probe — CHISON Medical Technologies Co., Ltd. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Boot Remedy Ltd

Sources (1)

FDA UDI 9af89258-6548-4368-ac3e-57595db131ca 33 fields · synced Jun 1, 2026