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VENTANA Protease Negative Reagent Control

FDA UDI

Class I (US FDA UDI)

by Ventana Medical Systems

Identity

Trade Name
VENTANA Protease Negative Reagent Control FDA UDI
Generic Name
Immunohistochemistry protease reagent IVD FDA UDI
Model / Reference
08129088001 FDA UDI

Identifiers

Catalog Number
08129088001 FDA UDI
Primary DI / UDI-DI
07613336141960 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Immunohistochemistry protease reagent IVD 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Immunohistochemistry protease reagent IVD

VENTANA Protease Negative Reagent Control by Ventana Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry protease reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b7e9291-afe1-4fbb-b813-72aaa97ee024 33 fields · synced May 31, 2026