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VinehealthPRO

FDA UDI

Class I (US FDA UDI)

by Vinehealth Digital Limited

Identity

Trade Name
VinehealthPRO FDA UDI
Generic Name
Clinical management support software FDA UDI
Model / Reference
R1 V3 FDA UDI

Identifiers

Primary DI / UDI-DI
05070000764122 FDA UDI
FDA Product Code
NXQ FDA UDI
GMDN Term
Clinical management support software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

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: Clinical management support software

VinehealthPRO by Vinehealth Digital Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical management support software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eff8173a-3766-468d-b225-f82f24149000 32 fields · synced May 30, 2026