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PATHWAY HER-2 4 in 1 Control Slides

FDA UDI

Class I (US FDA UDI)

by Ventana Medical Systems

Identity

Trade Name
PATHWAY HER-2 4 in 1 Control Slides FDA UDI
Generic Name
Human epidermal growth factor receptor 2 (HER2) protein IVD, control FDA UDI
Model / Reference
10 slides FDA UDI

Identifiers

Primary DI / UDI-DI
04015630972289 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Human epidermal growth factor receptor 2 (HER2) protein IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 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

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Human epidermal growth factor receptor 2 (HER2) protein IVD, control

PATHWAY HER-2 4 in 1 Control Slides by Ventana Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Human epidermal growth factor receptor 2 (HER2) protein IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e65ba0d3-2e86-4266-9f15-ca5eb730a812 32 fields · synced May 30, 2026