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Vivifyhealth SK011

FDA UDI

Class II (US FDA UDI)

by Vivify Health, Inc.

Identity

Trade Name
Vivifyhealth SK011 FDA UDI
Generic Name
Multiparameter physiologic analysis workstation FDA UDI
Device Name
Service Kit for A&D bariatric UA-789AC FDA UDI
Model / Reference
SK011 FDA UDI
Description
Service Kit for A&D bariatric UA-789AC FDA UDI

Identifiers

Primary DI / UDI-DI
00850032055253 FDA UDI
FDA Product Code
DRG FDA UDI
GMDN Term
Multiparameter physiologic analysis workstation 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiparameter physiologic analysis workstation

Vivifyhealth SK011 by Vivify Health, Inc. — Class II — 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
Vivify Health, Inc.

Sources (1)

  • FDA UDI fd7f5406-ba31-4c85-83f2-6c8d72b2a780 33 fields · synced May 30, 2026