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A&D Medical

FDA UDI

Class II (US FDA UDI)

by A & D Co., Ltd.

Identity

Trade Name
A&D Medical FDA UDI
Generic Name
Manual-inflation electronic sphygmomanometer, non-portable FDA UDI
Device Name
Digital Blood Pressure Monitor. FDA UDI
Model / Reference
UA-705 FDA UDI
Description
Digital Blood Pressure Monitor. FDA UDI

Identifiers

Catalog Number
UA-705V FDA UDI
Primary DI / UDI-DI
00093764601576 FDA UDI
510(k) Number
K032499 FDA UDI
FDA Product Code
DXN FDA UDI
GMDN Term
Manual-inflation electronic sphygmomanometer, non-portable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1130 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

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: Manual-inflation electronic sphygmomanometer, non-portable

A&D Medical by A & D Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual-inflation electronic sphygmomanometer, non-portable.

Cleared under the same submission

K032499 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A & D Co., Ltd.

Sources (1)

  • FDA UDI 9d607ef3-4ab5-4602-a991-bd8e1608368c 37 fields · synced Jun 8, 2026