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T-POC TOTAL IgE IMMUNOASSAY KIT

FDA UDI

by Axim Biotechnologies, Inc.

Identity

Trade Name
T-POC TOTAL IgE IMMUNOASSAY KIT FDA UDI
Generic Name
Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing FDA UDI
Device Name
LFIA kit for detection of IgE level in tear fluid. FDA UDI
Model / Reference
CP0001 FDA UDI
Description
LFIA kit for detection of IgE level in tear fluid. FDA UDI

Identifiers

Catalog Number
CP0001 FDA UDI
Primary DI / UDI-DI
00860009215139 FDA UDI
GMDN Term
Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing

T-POC TOTAL IgE IMMUNOASSAY KIT by Axim Biotechnologies, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a49552fe-1cba-40c9-a757-bfcc913d4b56 34 fields · synced May 30, 2026