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Bovie

FDA UDI

Class II (US FDA UDI)

by Bovie Medical Corporation

Identity

Trade Name
Bovie FDA UDI
Generic Name
Foetal Doppler system FDA UDI
Device Name
ACUDOP II 770, DISPLAY UNIT WITH 2MHZ OB WATERPROOF PROBE FDA UDI
Model / Reference
AD-770-A2W FDA UDI
Description
ACUDOP II 770, DISPLAY UNIT WITH 2MHZ OB WATERPROOF PROBE FDA UDI

Identifiers

Catalog Number
AD-770-A2W FDA UDI
Primary DI / UDI-DI
10607151011588 FDA UDI
510(k) Number
K090465 FDA UDI
FDA Product Code
ITX FDA UDI
LXE FDA UDI
GMDN Term
Foetal Doppler system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
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

Bovie by Bovie Medical Corporation — 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 b2cdfb27-6d54-4d11-9461-fd234babd93a 36 fields · synced Jun 8, 2026