← Back to catalogue

Endogenous Biotin Blocking Kit

FDA UDI

Class I (US FDA UDI)

by Ventana Medical Systems

Identity

Trade Name
ENDOGENOUS BIOTIN BLOCKING KIT FDA UDI
Generic Name
Immunohistochemistry endogenous avidin/biotin dual blocking reagent IVD FDA UDI
Model / Reference
05266092001 FDA UDI

Identifiers

Catalog Number
05266092001 FDA UDI
Primary DI / UDI-DI
04015630971282 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Immunohistochemistry endogenous avidin/biotin dual blocking 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Immunohistochemistry endogenous avidin/biotin dual blocking reagent IVD

Endogenous Biotin Blocking Kit by Ventana Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry endogenous avidin/biotin dual blocking reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Ventana Medical Systems

Sources (1)

  • FDA UDI 4ea5fc2a-130a-4b80-8256-ebfe21f52fc0 33 fields · synced May 31, 2026