← Back to catalogue

Antiserum to Human IgM

FDA UDI

Class II (US FDA UDI)

by Helena Laboratories, Corp.

Identity

Trade Name
Antiserum to Human IgM FDA UDI
Generic Name
Immunoglobulin M subclass (IgM subclass) IVD, reagent FDA UDI
Model / Reference
9234 FDA UDI

Identifiers

Primary DI / UDI-DI
M52592340 FDA UDI
FDA Product Code
CFF FDA UDI
GMDN Term
Immunoglobulin M subclass (IgM 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 M subclass (IgM subclass) IVD, reagent

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

Similar devices

Also classified as Immunoglobulin M subclass (IgM subclass) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 06f7b348-f3bb-4d85-9dd9-3e79780242a0 33 fields · synced Jun 9, 2026