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SureFISH 13q14.2 RB1 522kb P20 GR

FDA UDI

Class I (US FDA UDI)

by Agilent Technologies Inc.

Identity

Trade Name
SureFISH 13q14.2 RB1 522kb P20 GR FDA UDI
Generic Name
Nucleic acid hybridization detection IVD, reagent FDA UDI
Device Name
SureFISH 13q14.2 RB1 522kb P20 GR FDA UDI
Model / Reference
G110283G FDA UDI
Description
SureFISH 13q14.2 RB1 522kb P20 GR FDA UDI

Identifiers

Primary DI / UDI-DI
05700574037420 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Nucleic acid hybridization detection IVD, reagent 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: Nucleic acid hybridization detection IVD, reagent

SureFISH 13q14.2 RB1 522kb P20 GR by Agilent Technologies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid hybridization detection IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agilent Technologies Inc.

Sources (1)

  • FDA UDI f0ed9184-0e41-4641-941b-a8fadb066b90 36 fields · synced May 30, 2026