FDA UDI In Commercial Distribution 🇺🇸 United States

ProCheck

DI: 00642632747009 · Model: BP3KV1-5WPC · MICROLIFE USA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
ProCheck
Primary DI
00642632747009
Version / Model
BP3KV1-5WPC
Company Name
MICROLIFE USA, INC.
Labeler DUNS
176387785
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-16
Public Version
1
Public Version Date
2024-08-26
Public Version Status
New
Public Device Record Key
a4f6b185-acae-4ecb-98fe-53af994d70e4

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

GMDN Terms

Code Name
45617 Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

Identifiers

Type ID
Package 10642632747006
Primary 00642632747009
Package 20642632747003