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IDEAL LIFE BP-Manager™

FDA UDI

Class II (US FDA UDI)

by Ideal Life, Inc.

Identity

Trade Name
IDEAL LIFE BP-Manager™ FDA UDI
Generic Name
Manual-inflation electronic sphygmomanometer, portable FDA UDI
Model / Reference
BPM 0001 FDA UDI

Identifiers

Primary DI / UDI-DI
10804084000010 FDA UDI
510(k) Number
K060504 FDA UDI
FDA Product Code
DRG FDA UDI
DXN FDA UDI
GMDN Term
Manual-inflation electronic sphygmomanometer, portable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2910 FDA UDI
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

Dimensions & Sizes

Size
Weight — 429 Gram FDA UDI
Height — 57 Millimeter FDA UDI
Width — 94 Millimeter FDA UDI
Length — 154 Millimeter FDA UDI

Category: Manual-inflation electronic sphygmomanometer, portable

IDEAL LIFE BP-Manager™ by Ideal Life, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual-inflation electronic sphygmomanometer, portable.

Cleared under the same submission

K060504 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ideal Life, Inc.

Sources (1)

  • FDA UDI 7b7a3846-3d51-4f90-807c-246330d8f295 36 fields · synced May 30, 2026