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Blood Pressure Cuff

FDA UDI

Class II (US FDA UDI)

by Fresenius Medical Care

Identity

Trade Name
Blood Pressure Cuff FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
BPM cuff, 340 to 500 mm, size L FDA UDI
Model / Reference
F40016610 FDA UDI
Description
BPM cuff, 340 to 500 mm, size L FDA UDI

Identifiers

Primary DI / UDI-DI
04039361207960 FDA UDI
510(k) Number
K150708 FDA UDI
K173972 FDA UDI
K231125 FDA UDI
K243237 FDA UDI
K243505 FDA UDI
FDA Product Code
KDI FDA UDI
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5860 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 340 Millimeter FDA UDI
Length — 500 Millimeter FDA UDI

Category: Blood pressure cuff, reusable

Blood Pressure Cuff by Fresenius Medical Care — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3e33fa34-dcf2-47e8-adc6-f08b02abd4f8 36 fields · synced May 31, 2026