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DigiDop

FDA UDI

Class II (US FDA UDI)

by Newman Medical

Identity

Trade Name
DigiDop FDA UDI
Generic Name
Foetal Doppler system FDA UDI
Device Name
DigiDop 300, non-display, 2MHZ OB WATERPROOF FDA UDI
Model / Reference
DD-300-D2W FDA UDI
Description
DigiDop 300, non-display, 2MHZ OB WATERPROOF FDA UDI

Identifiers

Catalog Number
DD-300-D2W FDA UDI
Primary DI / UDI-DI
00852785008012 FDA UDI
510(k) Number
K090465 FDA UDI
FDA Product Code
LXE 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Foetal Doppler system

DigiDop by Newman Medical — 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

Manufacturer
Newman Medical

Sources (1)

  • FDA UDI 6c06a223-ff8e-4710-9114-40913d159fff 37 fields · synced May 30, 2026