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NexES Dispenser Card Option 1

FDA UDI

Class I (US FDA UDI)

by Ventana Medical Systems

Identity

Trade Name
NexES Dispenser Card Option 1 FDA UDI
Generic Name
Assay container IVD, single-use FDA UDI
Model / Reference
05271843001 FDA UDI

Identifiers

Catalog Number
05271843001 FDA UDI
Primary DI / UDI-DI
07613336125007 FDA UDI
FDA Product Code
JRC FDA UDI
GMDN Term
Assay container IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assay container IVD, single-use

NexES Dispenser Card Option 1 by Ventana Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assay container IVD, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36bfe366-0b57-450b-bac6-d8cf976017bc 33 fields · synced Jun 1, 2026