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Sensinel™ Cpm Base Station

FDA UDI

Class II (US FDA UDI)

by Analog Devices, Inc.

Identity

Trade Name
SENSINEL™ CPM BASE STATION FDA UDI
Generic Name
Wearable multiple vital physiological parameter monitoring system FDA UDI
Model / Reference
ADCP-1100-BS-001 FDA UDI

Identifiers

Primary DI / UDI-DI
00860006382339 FDA UDI
FDA Product Code
MWI FDA UDI
BZQ FDA UDI
DPS FDA UDI
DQD FDA UDI
DSB FDA UDI
DXH FDA UDI
FLL FDA UDI
GMDN Term
Wearable multiple vital physiological parameter monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
868.2375 FDA UDI
870.2340 FDA UDI
870.1875 FDA UDI
870.2770 FDA UDI
870.2920 FDA UDI
880.2910 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Wearable multiple vital physiological parameter monitoring system

Sensinel™ Cpm Base Station by Analog Devices, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wearable multiple vital physiological parameter monitoring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Analog Devices, Inc.

Sources (1)

  • FDA UDI 72d11599-7b5d-4204-922b-7dfdb8d42ed3 33 fields · synced May 30, 2026