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Cognito Health

FDA UDI

Class I (US FDA UDI)

by Cognito Health Inc.

Identity

Trade Name
Cognito Health FDA UDI
Generic Name
Bed/chair occupant movement pressure/vibration sensor FDA UDI
Model / Reference
P7FD-21 FDA UDI

Identifiers

Primary DI / UDI-DI
04719889980018 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Bed/chair occupant movement pressure/vibration sensor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bed/chair occupant movement pressure/vibration sensor

Cognito Health by Cognito Health Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed/chair occupant movement pressure/vibration sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cognito Health Inc.

Sources (1)

  • FDA UDI 44c27629-5b36-4df4-9eef-140ec585aa79 32 fields · synced May 30, 2026