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2-Compnent DAB Pack

FDA UDI

Class I (US FDA UDI)

by Biogenex Laboratories, Inc.

Identity

Trade Name
2-Compnent DAB Pack FDA UDI
Generic Name
Immunohistochemistry chromogenic substrate IVD, kit, enzyme immunohistochemistry FDA UDI
Model / Reference
HK542-XAKE FDA UDI

Identifiers

Catalog Number
HK542-XAKE FDA UDI
Primary DI / UDI-DI
00850646007365 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Immunohistochemistry chromogenic substrate IVD, kit, enzyme immunohistochemistry 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 chromogenic substrate IVD, kit, enzyme immunohistochemistry

2-Compnent DAB Pack by Biogenex Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry chromogenic substrate IVD, kit, enzyme immunohistochemistry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 87fae5bb-d9e6-47e0-b5f5-479a13c5d814 35 fields · synced May 30, 2026