← Back to catalogue

Finapres

FDA UDI

Class II (US FDA UDI)

by Finapres Medical Systems B.V.

Identity

Trade Name
Finapres FDA UDI
Generic Name
Patient monitoring system module, blood pressure, noninvasive FDA UDI
Device Name
FM Frontend Unit FDA UDI
Model / Reference
FM Frontend Unit FDA UDI
Description
FM Frontend Unit FDA UDI

Identifiers

Catalog Number
FP_905803 FDA UDI
Primary DI / UDI-DI
08719327003725 FDA UDI
510(k) Number
K023723 FDA UDI
K063111 FDA UDI
FDA Product Code
DSB FDA UDI
DXN FDA UDI
GMDN Term
Patient monitoring system module, blood pressure, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 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

No

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: Patient monitoring system module, blood pressure, noninvasive

Finapres by Finapres Medical Systems B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, blood pressure, noninvasive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 251aa809-2c6f-45d1-8bd2-2f9a4d2e7bfe 35 fields · synced May 31, 2026