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Sensinel™ Cpm Replacement Adhesive Pad

FDA UDI

Class II (US FDA UDI)

by Analog Devices, Inc.

Identity

Trade Name
SENSINEL™ CPM REPLACEMENT ADHESIVE PAD FDA UDI
Generic Name
Wearable multiple vital physiological parameter monitoring system FDA UDI
Model / Reference
ADI-CS-200-001 FDA UDI

Identifiers

Primary DI / UDI-DI
00860006382308 FDA UDI
FDA Product Code
BZQ FDA UDI
DPS FDA UDI
DQD FDA UDI
DSB FDA UDI
DXH FDA UDI
FLL FDA UDI
MWI FDA UDI
GMDN Term
Wearable multiple vital physiological parameter monitoring system FDA UDI

Classification

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wearable multiple vital physiological parameter monitoring system

Sensinel™ Cpm Replacement Adhesive Pad 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 90808faa-cdc9-491d-b1b3-7180d1be253e 33 fields · synced May 30, 2026