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Antiserum to Human IgD

FDA UDI

Class II (US FDA UDI)

by Helena Laboratories, Corp.

Identity

Trade Name
Antiserum to Human IgD FDA UDI
Generic Name
Immunoglobulin D subclass (IgD subclass) IVD, reagent FDA UDI
Model / Reference
9249 FDA UDI

Identifiers

Primary DI / UDI-DI
M52592490 FDA UDI
FDA Product Code
CFF FDA UDI
GMDN Term
Immunoglobulin D subclass (IgD subclass) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5510 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

Yes

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: Immunoglobulin D subclass (IgD subclass) IVD, reagent

Antiserum to Human IgD by Helena Laboratories, Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunoglobulin D subclass (IgD subclass) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6eb86604-93f1-4105-b4b2-6f587f219622 33 fields · synced Jun 9, 2026