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OpsisDx

FDA UDI

Class II (US FDA UDI)

by Entopsis, Llc

Identity

Trade Name
OpsisDx FDA UDI
Generic Name
Multiple-type clinical chemistry analyte profile IVD, reagent FDA UDI
Device Name
Four NuTec slides used to create bio-molecular profiles of samples FDA UDI
Model / Reference
NuTec Chamber FDA UDI
Description
Four NuTec slides used to create bio-molecular profiles of samples FDA UDI

Identifiers

Catalog Number
ENT001 FDA UDI
Primary DI / UDI-DI
B550ENT0010 FDA UDI
FDA Product Code
NSU FDA UDI
GMDN Term
Multiple-type clinical chemistry analyte profile IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.2570 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

OpsisDx by Entopsis, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Entopsis, Llc

Sources (1)

  • FDA UDI 1edfd58f-d410-4348-be04-225ed78c0d40 35 fields · synced May 30, 2026