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Chromosome 10 DIG Probe ASR

FDA UDI

Class I (US FDA UDI)

by Ventana Medical Systems

Identity

Trade Name
Chromosome 10 DIG Probe ASR FDA UDI
Generic Name
Assay development analyte-specific reagent IVD FDA UDI
Model / Reference
06577571001 FDA UDI

Identifiers

Catalog Number
06577571001 FDA UDI
Primary DI / UDI-DI
04015630970841 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Assay development analyte-specific reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

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: Assay development analyte-specific reagent IVD

Chromosome 10 DIG Probe ASR by Ventana Medical Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assay development analyte-specific reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ventana Medical Systems

Sources (1)

  • FDA UDI eb3f64a0-4c07-4072-9b51-0d4b86b4886c 33 fields · synced May 30, 2026