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Mumps IgM Control

FDA UDI

Class I (US FDA UDI)

by Bion Enterprises, Ltd.

Identity

Trade Name
Mumps IgM Control FDA UDI
Generic Name
Mumps virus immunoglobulin M (IgM) antibody IVD, control FDA UDI
Model / Reference
MUM-8030 FDA UDI

Identifiers

Catalog Number
MUM-8030 FDA UDI
Primary DI / UDI-DI
B110MUM80300 FDA UDI
510(k) Number
K894624 FDA UDI
FDA Product Code
GRA FDA UDI
GMDN Term
Mumps virus immunoglobulin M (IgM) antibody IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.3380 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mumps virus immunoglobulin M (IgM) antibody IVD, control

Mumps IgM Control by Bion Enterprises, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mumps virus immunoglobulin M (IgM) antibody IVD, control.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4fb6fa5f-ffaa-4141-b2bb-2a85633e3a90 36 fields · synced Jun 8, 2026