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Vivifyhealth SK010

FDA UDI

Class II (US FDA UDI)

by Vivify Health, Inc.

Identity

Trade Name
Vivifyhealth SK010 FDA UDI
Generic Name
Multiparameter physiologic analysis workstation FDA UDI
Device Name
Service Kit for glucose meters, lancets, and strips FDA UDI
Model / Reference
SK010 FDA UDI
Description
Service Kit for glucose meters, lancets, and strips FDA UDI

Identifiers

Primary DI / UDI-DI
00850032055239 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

Yes

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 SK010 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 8ba91beb-8283-487c-9b19-05fb0947186f 34 fields · synced Jun 1, 2026