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Mumps 10 Well - 10 pk

FDA UDI

Class I (US FDA UDI)

by Scimedx Corp.

Identity

Trade Name
Mumps 10 Well; 10 pk FDA UDI
Generic Name
Mumps virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay FDA UDI
Model / Reference
I-MUV01X FDA UDI

Identifiers

Catalog Number
I-MUV01X FDA UDI
Primary DI / UDI-DI
00813545026059 FDA UDI
FDA Product Code
GRA FDA UDI
GMDN Term
Mumps virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay FDA UDI
Models / Variants
Mumps 10 Well FDA UDI
10 pk 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mumps virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay

Mumps 10 Well - 10 pk by Scimedx Corp. — Class I — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

Similar devices

Also classified as Mumps virus immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Scimedx Corp.

Sources (1)

  • FDA UDI 90b4d5c4-ce2f-41ee-a8a3-6318d483f18a 34 fields · synced May 31, 2026