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ihc Enhancer 15mL

FDA UDI

Class I (US FDA UDI)

by Novodiax, Inc.

Identity

Trade Name
ihc Enhancer 15mL FDA UDI
Generic Name
Immunohistochemistry conjugated secondary antibody IVD FDA UDI
Model / Reference
D28020-R015 FDA UDI

Identifiers

Catalog Number
K51011-015 & K51011-030 FDA UDI
Primary DI / UDI-DI
00850030934604 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Immunohistochemistry conjugated secondary antibody 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

Dimensions & Sizes

Size
Total Volume — 15 Milliliter FDA UDI

Category: Immunohistochemistry conjugated secondary antibody IVD

ihc Enhancer 15mL by Novodiax, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry conjugated secondary antibody IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novodiax, Inc.

Sources (1)

  • FDA UDI fa4dbbb9-82bc-4795-988d-028d8b213faf 36 fields · synced Jun 1, 2026