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pGOLD Slides

FDA UDI

Class I (US FDA UDI)

by Nirmidas Biotech, Inc.

Identity

Trade Name
pGOLD Slides FDA UDI
Generic Name
Microplate IVD FDA UDI
Device Name
5-slide packaging FDA UDI
Model / Reference
NBPG-0005 FDA UDI
Description
5-slide packaging FDA UDI

Identifiers

Primary DI / UDI-DI
00860007960611 FDA UDI
FDA Product Code
KEW FDA UDI
GMDN Term
Microplate IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microplate IVD

pGOLD Slides by Nirmidas Biotech, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microplate IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nirmidas Biotech, Inc.

Sources (1)

  • FDA UDI 8e0d447b-d412-44b7-be48-df8957228049 33 fields · synced May 30, 2026