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intelliPATH FLX™ Fast Red Chromogen Kit

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref IPK5017G80Model Warp Red Chromogen Kits for IHC

by Biocare Medical, Llc

Identity

Trade Name
intelliPATH FLX™ DAB Chromogen Kit, 80mL EUDAMED
intelliPATH FLX™ Fast Red Chromogen Kit FDA UDI
Generic Name
Immunohistochemistry chromogenic substrate IVD, kit, enzyme immunohistochemistry FDA UDI
Device Name
Warp Red Chromogen Kits for IHC EUDAMED
Model / Reference
IPK5017G80 EUDAMEDFDA UDI
Warp Red Chromogen Kits for IHC EUDAMED

Identifiers

Primary DI / UDI-DI
00847627009012 EUDAMEDFDA UDI
Basic UDI-DI
08476270BWR806J6 EUDAMED
FDA Product Code
NJT FDA UDI
EMDN Code
W01030799 HISTOLOGY / CYTOLOGY REAGENTS - OTHER EUDAMED
GMDN Term
Immunohistochemistry chromogenic substrate IVD, kit, enzyme immunohistochemistry FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

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 chromogenic substrate IVD, kit, enzyme immunohistochemistry

intelliPATH FLX™ Fast Red Chromogen Kit by Biocare Medical, Llc — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI d8acd2ab-9a77-42db-93ca-219d0c0783c9 33 fields · synced Jun 18, 2026
  • EUDAMED 8c5476a0-6e18-428a-9ce3-5fa379ff8ee3 61 fields · synced Jun 18, 2026