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Vital Sync

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
Vital Sync FDA UDI
Generic Name
Multiparameter physiologic analysis workstation FDA UDI
Device Name
Early Warning Score Application v1.0 FDA UDI
Model / Reference
EWS v1.0 FDA UDI
Description
Early Warning Score Application v1.0 FDA UDI

Identifiers

Primary DI / UDI-DI
10884521706668 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Multiparameter physiologic analysis workstation FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiparameter physiologic analysis workstation

Vital Sync by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiparameter physiologic analysis workstation.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 97ca23b4-7801-4111-aeb9-8662fb0ef8da 34 fields · synced Jun 6, 2026