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Platelia

FDA UDI

Class I (US FDA UDI)

by Bio-Rad

Identity

Trade Name
Platelia FDA UDI
Generic Name
Aspergillus fumigatus immunoglobulin G (IgG) antibody IVD, control FDA UDI
Device Name
Platelia Aspergillus IgG - negative and positive controls FDA UDI
Model / Reference
62786 FDA UDI
Description
Platelia Aspergillus IgG - negative and positive controls FDA UDI

Identifiers

Catalog Number
62786 FDA UDI
Primary DI / UDI-DI
03610520002490 FDA UDI
FDA Product Code
KFG FDA UDI
GMDN Term
Aspergillus fumigatus immunoglobulin G (IgG) antibody IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3040 FDA UDI
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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Aspergillus fumigatus immunoglobulin G (IgG) antibody IVD, control

Platelia by Bio-Rad — Class I — 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

Manufacturer
Bio-Rad

Sources (1)

  • FDA UDI 645cfb0c-4477-48c1-9f19-dd097ec7bb78 37 fields · synced Jun 8, 2026