FDA UDI In Commercial Distribution 🇺🇸 United States

InBody

DI: 08809209590822 · Model: BPBIO210 · InBody Co., Ltd.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
InBody
Primary DI
08809209590822
Version / Model
BPBIO210
Company Name
InBody Co., Ltd.
Labeler DUNS
688003404
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-25
Public Version
1
Public Version Date
2022-08-02
Public Version Status
New
Public Device Record Key
4973606d-050a-41fe-8eac-4449eb918e10

Device Description

The subject device is a manual blood pressure (BP) monitor, and requires the user to listen for Korotkoff sounds to determine systolic and diastolic pressure. Further, patients whose Korotkoff sounds are not clear or absent, such as children younger than 3 years of age, will not be suitable for the subject device. Pulse rate is also measured.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Lot/Batch Number
No
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
DXQ Blood Pressure Cuff

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Primary 08809209590822

Customer Contacts

Phone
323-932-6503

Premarket Submissions

Submission Number Supplement Number
K200560 000