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DxSelect™ Sample Diluent

FDA UDI

Class II (US FDA UDI)

by DiaSorin Molecular LLC

Identity

Trade Name
DxSelect™ Sample Diluent FDA UDI
Generic Name
Immunohistochemistry antibody diluent IVD FDA UDI
Model / Reference
EL1608 FDA UDI

Identifiers

Catalog Number
EL1608 FDA UDI
Primary DI / UDI-DI
10816101022226 FDA UDI
510(k) Number
K993754 FDA UDI
FDA Product Code
MXJ FDA UDI
GMDN Term
Immunohistochemistry antibody diluent IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3305 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: Immunohistochemistry antibody diluent IVD

DxSelect™ Sample Diluent by DiaSorin Molecular LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry antibody diluent IVD.

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 698e7207-3400-4e38-afe0-77ec66718ae9 36 fields · synced Jun 9, 2026