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Sensium Vitals

FDA UDI

Class II (US FDA UDI)

by Sensium Healthcare Limited

Identity

Trade Name
Sensium Vitals FDA UDI
Generic Name
Nurse call system FDA UDI
Model / Reference
US Patch FDA UDI

Identifiers

Catalog Number
TZ202055 FDA UDI
Primary DI / UDI-DI
05060403780041 FDA UDI
510(k) Number
K110809 FDA UDI
FDA Product Code
DRG FDA UDI
GMDN Term
Nurse call system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Nurse call system

Sensium Vitals by Sensium Healthcare Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nurse call system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sensium Healthcare Limited

Sources (1)

  • FDA UDI 80cb57b7-362d-4d8e-9a59-7727cae8f35b 36 fields · synced May 30, 2026