Device
This Blood Pressure Cuff is a non-invasive blood pressure cuff, intended for use in conjunction with non-automated and automated
Manufacturer
Fysicon B.V.
Fysicon B.V.
Model: QMAPP NiBP Connection hose 365 cm
Catalog: 01567082
DI: 08719689142605
Status: New
MRI: Labeling does not contain MRI Safety Information
Single-use: No
Rx: Yes
OTC: No
First Published: 2026-05-19
Current Version: 2026-05-27
Description
This Blood Pressure Cuff is a non-invasive blood pressure cuff, intended for use in conjunction with non-automated and automated
sphygmomanometers, such as QMAPP, to determine blood pressure in pediatric through adult patients. The QMAPP NiBP
connection hose, is a hose that interconnects a reusable or disposable NiBP cuff to a QMAPP amplifier.
This NiBP connection hose or cuff is reusable, unless otherwise stated.
Sterilization
Device Sterile:
No
Sterilization Prior To Use:
No
Regulatory & Distribution
Record Status:
Published
Version Number:
1
Record Key:
99f8648f-9e2a-4211-882d-5529387005dc
Distribution Status:
In Commercial Distribution
DUNS Number:
404866654
Device Count:
1
DM Exempt:
No
Premarket Exempt:
No
HCT/P:
No
Kit:
No
Combination Product:
No
Lot/Batch Tracked:
Yes
Serial Number Tracked:
No
Manufacturing Date Tracked:
Yes
Expiration Date Tracked:
No
Donation ID Number Tracked:
No
Labeled Contains NRL:
No
Labeled No NRL:
No
Identifiers
Device ID:
08719689142605
Type:
Primary
Issuing Agency:
GS1
GMDN
Code: 67106
Name: Multiple physiological parameter monitoring support kit
Definition:
A collection of noninvasive devices intended to be used in conjunction with a parent physiological parameter monitor for enabling measurement of multiple vital parameters [e.g., electrocardiogram (ECG), noninvasive blood pressure (NIBP), temperature]. It typically includes an inflatable blood pressure cuff, patient temperature probe, and electrical cables for connection to the monitor (e.g., for connecting an ECG lead to the monitor). This is a reusable device.
FDA Product Codes
DSA
Cable, Transducer And Electrode, Patient, (Including Connector)
Premarket Submissions
Submission Number:
K241766
Supplement Number:
000